👉 Explore the Course on Udemy
Are you looking for pharmaceutical jobs in Pune? Centaur Pharmaceuticals Walk-In Interview 2026 offers an opportunity for experienced pharmaceutical professionals to explore Quality Assurance (QA) and Quality Control (QC) positions at its formulation manufacturing facility in Hinjewadi, Pune.
According to the recruitment information provided, Centaur Pharmaceuticals Pvt. Ltd. is conducting a walk-in interview on 1 November 2026 for multiple positions ranging from officer-level roles to assistant manager and deputy manager positions.
Candidates with qualifications such as B.Pharm, M.Pharm, and M.Sc, along with relevant experience in pharmaceutical manufacturing, quality systems, analytical testing, and regulatory compliance, may find these opportunities worth exploring.
The vacancies cover areas such as IT Quality Assurance (ITQA), Quality Management Systems (QMS), equipment qualification, validation, HPLC and GC analysis, laboratory information management systems (LIMS), stability studies, and analytical method validation.
Read on for the available positions, qualifications, experience requirements, interview schedule, venue, and application procedure.
Important: The recruitment details below are based on the information provided for this post. Candidates should confirm the vacancies, interview schedule, contact details, and eligibility criteria with the company before attending. Independent verification of the announcement has not been completed.
Centaur Pharmaceuticals Walk-In Interview 2026: Overview
| Particulars | Details |
|---|---|
| Company Name | Centaur Pharmaceuticals Pvt. Ltd. |
| Recruitment Type | Walk-In Interview |
| Job Category | Pharmaceutical Jobs |
| Departments | Quality Assurance (QA) and Quality Control (QC) |
| Job Location | Hinjewadi Phase II, Pune, Maharashtra |
| Interview Date | 1 November 2026, Sunday |
| Interview Time | 8:30 AM onwards |
| Qualifications | B.Pharm, M.Pharm, and M.Sc, depending on the position |
| Experience Required | Approximately 3–16 years, depending on the position |
| Industry | Pharmaceutical Manufacturing |
| Application Mode | Walk-in interview / email, subject to confirmation |
| HR Email | go to apply page |
| Contact Number | +91-20-66739510 |
About Centaur Pharmaceuticals
Centaur Pharmaceuticals Pvt. Ltd. is a pharmaceutical company operating in the healthcare and pharmaceutical manufacturing sector.
Quality Assurance and Quality Control professionals play important roles in pharmaceutical manufacturing by maintaining product quality, ensuring compliance with applicable regulatory requirements, and supporting reliable manufacturing and laboratory operations.
Professionals working in regulated pharmaceutical facilities may be involved in documentation, investigations, validation activities, analytical testing, stability studies, laboratory data integrity, and regulatory inspections.
The recruitment information provided for this drive refers to a formulation manufacturing facility in Hinjewadi, Pune, and includes positions requiring relevant experience in regulated manufacturing environments.
Candidates should verify the facility’s current regulatory approval status and the specific requirements of each vacancy before applying.
1. Quality Assurance (QA) Vacancies at Centaur Pharmaceuticals
The Quality Assurance department helps ensure that pharmaceutical manufacturing activities comply with established quality systems, approved procedures, and applicable regulatory requirements.
According to the supplied recruitment details, the following positions are available for experienced candidates.
A. Executive / Senior Executive – IT Quality Assurance (ITQA)
Qualification: B.Pharm, M.Pharm, or M.Sc
Experience: 6–10 years
Department: Quality Assurance
This position is intended for professionals with experience in IT Quality Assurance and computerized systems used in pharmaceutical operations.
Potential responsibilities may include:
- Supporting computerized system validation activities.
- Reviewing system validation documentation.
- Maintaining compliance with applicable electronic records and electronic signatures requirements.
- Supporting data integrity assessments.
- Reviewing system access controls and audit trails.
- Coordinating with IT, Quality Assurance, and other departments.
- Supporting internal and external audits.
Candidates with relevant experience in computerized system validation, pharmaceutical quality systems, and data integrity may be suitable for this position.
B. Assistant Manager / Deputy Manager – QMS & Analytical QA
Qualification: B.Pharm, M.Pharm, or M.Sc
Experience: 12–16 years
Department: Quality Assurance
This position is intended for experienced professionals with expertise in Quality Management Systems and analytical Quality Assurance.
Potential responsibilities include:
- Managing quality investigations and deviations.
- Conducting root cause analysis.
- Reviewing and monitoring Corrective and Preventive Actions (CAPA).
- Reviewing analytical laboratory documentation.
- Supporting change control processes.
- Monitoring quality metrics and recurring deviations.
- Coordinating responses to audit observations.
- Supporting continuous improvement initiatives.
Candidates should be prepared to discuss their experience with pharmaceutical quality systems, investigation management, documentation practices, and regulatory compliance.
C. Senior Officer / Executive – Qualification & Validation
Qualification: B.Pharm or M.Pharm
Experience: 5–10 years
Department: Quality Assurance
This position focuses on equipment qualification and validation activities within pharmaceutical manufacturing operations.
Potential responsibilities include:
- Preparing and reviewing qualification protocols.
- Supporting equipment qualification activities.
- Working on utility qualification and validation.
- Supporting process validation.
- Conducting cleaning validation activities.
- Preparing validation reports.
- Managing deviations identified during qualification and validation.
- Ensuring documentation complies with approved procedures.
Candidates with hands-on experience in pharmaceutical manufacturing validation and regulated facility documentation may consider applying.
2. Quality Control (QC) Vacancies at Centaur Pharmaceuticals
The Quality Control department supports pharmaceutical product quality through analytical testing, laboratory documentation, instrument management, and compliance with approved testing procedures.
The recruitment information lists the following QC positions.
A. Assistant Manager / Deputy Manager – QC Section Head
Qualification: M.Sc
Experience: 12–16 years
Department: Quality Control
The listed section head opportunities include:
- Raw Material (RM) Section Head
- Stability Section Head
- Analytical Method Validation / Transfer (AMV / AMT) Section Head
- Good Laboratory Practices (GLP) Section Head
The precise responsibilities will depend on the selected section.
Potential responsibilities include:
- Managing day-to-day laboratory operations.
- Reviewing analytical data and laboratory documentation.
- Monitoring laboratory compliance and performance.
- Supporting analytical method validation and transfer.
- Overseeing raw material testing and stability studies, where applicable.
- Managing laboratory investigations and CAPA.
- Ensuring adherence to approved testing procedures.
- Supporting regulatory inspections and audit readiness.
- Coordinating laboratory activities with other departments.
Candidates applying for leadership roles should be prepared to explain their experience in managing laboratory teams, handling investigations, reviewing analytical results, and maintaining compliance in regulated pharmaceutical environments.
B. Executive / Senior Executive – QC QMS
Qualification: M.Sc
Experience: 10–15 years
Department: Quality Control
This role focuses on Quality Management Systems within the analytical laboratory.
Potential responsibilities include:
- Managing laboratory deviations and investigations.
- Supporting root cause analysis and CAPA.
- Reviewing laboratory documentation.
- Monitoring compliance with approved procedures.
- Supporting change control activities.
- Tracking recurring quality issues.
- Coordinating audit preparation and responses.
- Maintaining laboratory quality records.
Candidates with substantial experience in laboratory quality systems and regulated pharmaceutical operations may be suitable.
C. Officer / Senior Officer – Instrument Handling
Qualification: M.Sc
Experience: 3–5 years
Department: Quality Control
Candidates with practical experience in analytical laboratory instruments may consider this position.
Relevant instruments may include:
- High-Performance Liquid Chromatography (HPLC)
- Gas Chromatography (GC)
- UV-Visible Spectrophotometers
- Other analytical instruments relevant to pharmaceutical testing
Potential responsibilities include:
- Operating analytical instruments.
- Performing routine laboratory testing.
- Supporting instrument troubleshooting.
- Maintaining instrument usage and maintenance records.
- Following approved analytical procedures.
- Supporting calibration and qualification activities as required.
- Maintaining laboratory documentation and data integrity.
- Reporting unexpected results or instrument issues according to established procedures.
Candidates should be prepared to discuss their practical experience with the instruments relevant to their previous roles.
D. Junior Executive / Executive – Instrument Testing
Qualification: M.Sc
Experience: 6–10 years
Department: Quality Control
This position focuses on analytical testing and method verification using laboratory instruments.
Potential responsibilities include:
- Performing routine and non-routine analytical testing.
- Operating HPLC and GC instruments.
- Following approved testing procedures.
- Reviewing chromatographic data.
- Supporting analytical method verification activities.
- Maintaining laboratory records.
- Reporting deviations and unexpected analytical results.
- Ensuring compliance with applicable laboratory procedures.
Candidates with experience in pharmaceutical analytical testing and laboratory documentation may find this opportunity relevant.
Note: The designation and experience combination should be confirmed with the recruiting team because the supplied information lists Junior Executive / Executive positions requiring 6–10 years of experience.
E. Officer / Senior Officer – LIMS Master & Specifications
Qualification: M.Sc
Experience: 3–5 years
Department: Quality Control
This position focuses on Laboratory Information Management System (LIMS) master data and analytical specifications.
Potential responsibilities include:
- Creating and maintaining LIMS master data.
- Setting up analytical specifications.
- Maintaining laboratory-related system information.
- Supporting controlled updates to master data.
- Checking the accuracy of specification entries.
- Maintaining appropriate documentation.
- Supporting system compliance and data integrity.
- Coordinating with laboratory and quality teams.
Candidates with experience in LIMS administration, laboratory specifications, and pharmaceutical quality documentation may consider applying.
F. Junior Executive / Executive – LIMS & Specification Reviewer
Qualification: M.Sc
Experience: 8–12 years
Department: Quality Control
This position focuses on reviewing laboratory specifications and related LIMS workflows.
Potential responsibilities include:
- Reviewing analytical specifications.
- Checking laboratory master data for accuracy.
- Reviewing LIMS workflows and associated documentation.
- Supporting data integrity requirements.
- Coordinating specification changes.
- Ensuring controlled documentation practices.
- Supporting audits and laboratory compliance activities.
Candidates should confirm the exact designation, reporting structure, and experience requirements with the recruiting team before attending.
3. Eligibility Criteria for Centaur Pharma Jobs 2026
Candidates should review the eligibility requirements carefully before applying.
Educational Qualifications
The supplied recruitment details list the following qualifications:
- B.Pharm: For selected Quality Assurance positions.
- M.Pharm: For selected Quality Assurance positions.
- M.Sc: For the listed Quality Control positions and certain Quality Assurance positions.
The accepted M.Sc specializations have not been specified for every vacancy. Candidates should confirm whether their specialization meets the requirements of the relevant role.
Work Experience
The listed positions require approximately 3–16 years of relevant professional experience.
Experience requirements vary by designation:
| Position Category | Listed Experience |
|---|---|
| IT Quality Assurance | 6–10 years |
| QMS & Analytical QA | 12–16 years |
| Qualification & Validation | 5–10 years |
| QC Section Head | 12–16 years |
| QC QMS | 10–15 years |
| QC Instrument Handling | 3–5 years |
| QC Instrument Testing | 6–10 years |
| LIMS Master & Specifications | 3–5 years |
| LIMS & Specification Reviewer | 8–12 years |
These requirements are reproduced from the supplied recruitment information and should be confirmed against the official vacancy notice.
Relevant Industry Experience
The supplied announcement specifies experience in regulated pharmaceutical manufacturing environments, particularly Oral Solid Dosage (OSD) facilities.
Candidates should confirm whether their previous manufacturing experience meets the company’s requirements.
Regulatory Audit Exposure
The recruitment information highlights exposure to regulatory audits, including those associated with:
- US Food and Drug Administration (USFDA)
- Medicines and Healthcare products Regulatory Agency (MHRA)
- European Union Good Manufacturing Practice (EU-GMP) requirements
Applicants should be ready to explain their actual responsibilities during audits, inspections, observations, and subsequent corrective actions.
Important: Do not assume that meeting the educational qualification alone is sufficient. Relevant experience and the specific technical requirements of the selected role may be essential.
4. Walk-In Interview Date, Time and Venue
Candidates interested in the listed vacancies should confirm the interview arrangements before travelling.
Interview Details
- Company: Centaur Pharmaceuticals Pvt. Ltd.
- Date: Sunday, 1 November 2026
- Time: 8:30 AM onwards
- Location: Hinjewadi Phase II, Pune, Maharashtra
Venue address provided in the recruitment information:
Centaur Pharmaceuticals Pvt. Ltd.
Plot No. 4, International Biotech Park
Hinjawadi Phase II
Pune, Maharashtra – 411057
Before attending: Confirm the address, reporting time, available positions, and whether the walk-in drive is proceeding as scheduled by contacting the company through a verified official channel.
Candidates travelling from outside Pune should confirm these details in advance.
5. How to Apply for Centaur Pharmaceuticals Recruitment 2026
According to the supplied recruitment information, candidates may attend the walk-in interview or enquire about submitting their applications by email.
Option 1: Attend the Walk-In Interview
Eligible candidates can prepare the required documents and attend the interview at the specified venue on 1 November 2026.
Before travelling:
- Confirm that the vacancy relevant to your experience is available.
- Verify the reporting time and interview venue.
- Update your resume with your latest work experience.
- Prepare a summary of your technical responsibilities.
- Carry supporting educational and employment documents.
- Prepare to discuss regulatory audits, investigations, validation, analytical testing, or other role-specific responsibilities.
Option 2: Apply Through Email
The following email address was supplied in the recruitment information:
Email: hrpune@centaur.co.in
👉 Explore the Course on Udemy
Before emailing your personal documents, verify the address through the company’s official website or a reliable recruitment announcement.
Suggested email subject:
Application for [Position Name] – [Department] – [Years of Experience]
Example:
Application for Senior Executive ITQA – Quality Assurance – 7 Years of Experience
Documents to Attach
Candidates may prepare the following documents, as applicable:
- Updated resume or CV
- Recent passport-size photograph, if requested
- Educational qualification certificates
- Relevant experience documents
- Current employment details
- Notice period information
- Current and expected CTC details, if requested
Avoid sending unnecessary sensitive personal or financial information in an initial application.
6. Documents to Carry for the Walk-In Interview
Candidates attending the interview should consider carrying:
- Updated resume with current contact details.
- Passport-size photographs, if requested.
- Copies of educational certificates.
- Experience letters or employment records.
- Recent salary slips, if available and requested.
- Identification document, if required for entry.
- Details of current CTC, expected CTC, and notice period.
- Relevant technical training certificates.
- A summary of previous responsibilities and major professional achievements.
Keep digital copies of important documents as a backup.
The recruiting team may specify additional documents depending on the position.
7. Interview Preparation Tips for QA and QC Professionals
Candidates should prepare according to the position they intend to apply for.
For Quality Assurance Candidates
Revise the following topics:
- Pharmaceutical Quality Management Systems
- Deviation management
- Root Cause Analysis (RCA)
- Corrective and Preventive Actions (CAPA)
- Change control
- Equipment qualification
- Process validation
- Cleaning validation
- Computerized System Validation (CSV)
- Data integrity and ALCOA+ principles
- Applicable electronic records requirements, including 21 CFR Part 11 where relevant
- Regulatory audit preparation and responses
For ITQA roles, focus on computerized systems, validation documentation, access controls, audit trails, and data integrity.
For qualification and validation roles, prepare examples of protocols, reports, deviations, and validation activities you have handled.
For Quality Control Candidates
Revise topics relevant to your laboratory experience:
- HPLC operation and troubleshooting
- GC operation and troubleshooting
- Analytical method validation
- Analytical method transfer
- Stability studies
- Raw material testing
- Laboratory documentation
- Laboratory investigations
- Out-of-Specification (OOS) results
- Out-of-Trend (OOT) results
- Good Laboratory Practices
- LIMS and specification management
- Laboratory data integrity
Candidates applying for section head roles should also prepare examples of team management, laboratory investigations, audit readiness, and quality improvement.
Prepare Real Examples From Your Experience
Interviewers may ask you to explain situations you have handled in previous employment.
Prepare concise examples covering:
- A significant deviation you investigated.
- A root cause you identified.
- A CAPA you implemented or monitored.
- An audit in which you participated.
- An analytical instrument issue you resolved.
- A validation activity you supported.
- A data integrity concern you addressed.
Clearly explain your individual contribution, the action you took, and the outcome.
8. Why Consider Quality Assurance and Quality Control Careers?
Quality Assurance and Quality Control are important career paths in pharmaceutical manufacturing.
Quality Assurance Career Opportunities
QA professionals may develop expertise in:
- Quality Management Systems
- Regulatory compliance
- Validation and qualification
- Computerized system validation
- Documentation and audit management
- Manufacturing quality oversight
With relevant experience and demonstrated technical competence, professionals may progress into senior executive, managerial, and other leadership positions.
Quality Control Career Opportunities
QC professionals may develop expertise in:
- Analytical chemistry
- Instrumentation
- Method validation and transfer
- Stability testing
- Laboratory quality systems
- LIMS and laboratory data management
Professionals with strong analytical, documentation, and leadership skills may progress into senior laboratory and management roles.
Actual career progression depends on qualifications, experience, performance, and available opportunities.
9. Frequently Asked Questions (FAQs)
Q1. When is the Centaur Pharmaceuticals Walk-In Interview 2026?
According to the supplied recruitment information, the walk-in interview is scheduled for 1 November 2026, Sunday, at 8:30 AM onwards. Confirm the schedule before attending.
Q2. Where will the interview take place?
The supplied venue is Centaur Pharmaceuticals Pvt. Ltd., Plot No. 4, International Biotech Park, Hinjewadi Phase II, Pune, Maharashtra – 411057. Verify the address with the company before travelling.
Q3. Which departments are hiring?
The supplied information lists vacancies in Quality Assurance (QA) and Quality Control (QC).
Q4. What qualifications are required?
The listed qualifications include B.Pharm, M.Pharm, and M.Sc, depending on the role. Candidates should confirm the accepted qualifications and specializations for their selected position.
Q5. How much experience is required?
The supplied details list experience requirements ranging from approximately 3 to 16 years, depending on the designation.
Q6. Can freshers apply?
The supplied recruitment information lists experienced professional positions and does not specify vacancies for freshers. Candidates without relevant experience should confirm whether any entry-level opportunities are available.
Q7. Is experience in a regulated pharmaceutical facility required?
The supplied announcement highlights experience in regulated OSD manufacturing facilities and exposure to regulatory audits. Candidates should confirm these requirements with the recruiting team.
Q8. How can candidates apply by email?
The supplied recruitment information lists hrpune@centaur.co.in. Verify the email address through an official company source before sending your application.
Q9. What documents should candidates bring?
Candidates should prepare an updated resume, educational certificates, relevant experience documents, and any additional documents specified by the recruiting team.
Q10. Is the salary mentioned in the recruitment announcement?
The supplied information does not specify salary ranges for these positions. Candidates should enquire about the compensation structure during the recruitment process.
Q11. Are all the listed vacancies confirmed?
The positions and eligibility details in this post are based on the information provided for drafting. Candidates should verify current openings and designation-specific requirements with the company before making travel arrangements.
10. Final Words
The Centaur Pharmaceuticals Walk-In Interview 2026 may be worth exploring for experienced pharmaceutical professionals seeking Quality Assurance and Quality Control opportunities in Pune.
The supplied vacancy information covers several specialized areas, including ITQA, QMS, qualification and validation, analytical testing, stability, LIMS, and laboratory management.
Candidates should carefully match their qualifications and experience with the relevant position, prepare for technical questions, and verify the recruitment details before attending the interview.
If you are interested in pharmaceutical jobs in Pune, continue checking JobsOnTheWay.com for updates on Quality Assurance, Quality Control, Clinical Research, Regulatory Affairs, and other pharmaceutical career opportunities.
Disclaimer: This article is intended for job-information purposes. The vacancy details, interview schedule, eligibility requirements, venue, and contact information have not been independently verified. Recruitment plans may change. Confirm all important details with Centaur Pharmaceuticals through an official channel before applying or travelling.
Stay connected with JobsOnTheWay.com for the latest pharmaceutical job updates!