Category: Featured

Ipca Laboratories Limited is conducting a Walk-In Interview for freshers for its Center of Excellence (CoE) training initiative in the Production API department.
The program is designed to provide hands-on industrial exposure to students looking to build a career in the pharmaceutical industry.
Eligible B.Sc. Chemistry and B.Tech Chemical pass-outs can attend the walk-in interview for the Production API training program.
The three-month training includes a ₹12,300 monthly stipend, with career progression opportunities after successful completion of the program.

Ipca Laboratories Production API: Walk-In Interview Details

Ipca Laboratories Ltd. has launched its Center of Excellence (CoE) as a specialized training initiative aimed at providing practical industrial exposure to students aspiring to build a career in the pharmaceutical industry.

The program is designed to enhance participants’ practical understanding of the Production Department and prepare them for real-world applications in pharmaceutical manufacturing.

Ipca Laboratories Production API: Walk-In Interview Schedule

• Date: Saturday, 3rd October 2026
• Time: 10:00 AM to 16:00 hrs
• Venue: Ipca Laboratories Limited, Plot No. 16-22, Industrial Area No. 1, AB Road, Dewas, Madhya Pradesh

Ipca Laboratories Production API: Eligibility & Qualifications

Educational Qualification

Candidates meeting the following qualification criteria are eligible:

B.Sc. Chemistry | B.Tech. Chemical

• Pass-out year: 2023–2026
• The opportunity is intended for freshers interested in pharmaceutical production and API manufacturing.

Ipca Laboratories Production API: Training Details

Department

Production – API

Center of Excellence Training

The CoE training program provides participants with hands-on industrial exposure and practical understanding of pharmaceutical API production operations.

The training duration is 3 months.

Stipend

₹12,300 per month

Other Facilities

• Free canteen
• Transportation facility

Ipca Laboratories Production API: Career Progression

Upon successful completion of the 3-month CoE training program, candidates will be absorbed at Ipca Laboratories Ltd., Renukoot, Dewas API and Wardha API on CTC packages of:

• ₹2.55 LPA
• ₹2.65 LPA
• ₹3.45 LPA

The applicable CTC will depend on compatibility and skills.

How to Apply

Interested candidates should attend the walk-in interview with their updated resume.

Candidates are advised to carry the required documents and attend the interview at the specified venue and time.

Ipca Laboratories Recruitment Disclaimer

Ipca Laboratories Ltd. does not charge any fees from candidates at any stage of the recruitment process. Candidates should not respond to or make payments against recruitment-related requests.

Any demand for payment by a recruiter or agency claiming to represent Ipca Laboratories Ltd. should be reported immediately to:

ipca@ipca.com
corporate.communication@ipca.com

Job Summary

Sudeep Pharma Limited is hiring candidates for the Quality Control (QC) Department at its Nandesari GIDC facility in Vadodara.
The opening is for QC Trainee / QC Chemist with 0–2 years of experience, including freshers.
Candidates with a B.Sc. or M.Sc. in Chemistry can apply for this pharmaceutical quality control opportunity.
The role offers exposure to analytical testing, laboratory practices, GMP, GLP and data integrity requirements.

Sudeep Pharma Limited QC Trainee / QC Chemist

Sudeep Pharma Limited QC Department: Job Details

Company: Sudeep Pharma Limited
Department: Quality Control
Position: QC Trainee / QC Chemist
Location: Nandesari GIDC, Vadodara, Gujarat
Experience: 0–2 Years
Freshers: Can apply

Sudeep Pharma Limited QC Trainee / QC Chemist: Eligibility & Qualifications

Candidates with the following qualifications are eligible:

B.Sc. Chemistry | M.Sc. Chemistry

Sudeep Pharma Limited QC Trainee / QC Chemist: Desired Candidate Profile

• B.Sc. / M.Sc. in Chemistry.
• 0–2 years of experience in Pharmaceutical Quality Control.
• Freshers are encouraged to apply.
• Basic knowledge of analytical instruments and laboratory practices.
• Good communication skills and a willingness to learn.
• Team player with attention to detail.

Sudeep Pharma Limited QC Trainee / QC Chemist: Key Responsibilities

Quality Control Analysis

• Analysis of raw materials, in-process samples, finished products and stability samples.
• Operate analytical instruments such as UV, FTIR, KF and pH meter.
• Maintain analytical records and reports.
• Perform routine laboratory activities and support instrument calibration.

Sudeep Pharma Limited QC: GMP & Laboratory Compliance

• Ensure compliance with GMP and GLP requirements.
• Maintain data integrity in laboratory activities.
• Follow applicable laboratory procedures and documentation practices.
• Maintain attention to detail during testing and documentation.

Why Join Sudeep Pharma Limited QC Department?

The position provides an opportunity to work in a modern QC laboratory and develop practical pharmaceutical quality control skills. The organization highlights career growth opportunities, learning and development, and a supportive work culture.

How to Apply

Interested candidates can send their updated CV to:

Email: tanmay.talati@sudeepgroup.com

Candidates can apply by sending their updated resume to the above email address.

Job Summary

Kamla Lifesciences Ltd. is looking for dedicated and enthusiastic candidates to join its Ointment Manufacturing Unit.
The company is hiring Ointment Officers with experience in pharmaceutical manufacturing operations.
Candidates with B.Pharm or M.Pharm and 2 to 6 years of relevant experience can apply.
The position is based at Boisar, Tarapur, with male candidates preferred for the role.

Kamla Lifesciences Ointment Officer

Kamla Lifesciences Ointment Manufacturing: Job Details

Company: Kamla Lifesciences Ltd.
Department: Ointment Manufacturing
Designation: Ointment Officer
Location: Boisar, Tarapur
Experience: 2–6 Years
Candidate Preference: Male candidates preferred

Eligibility & Qualifications for Kamla Lifesciences Ointment Officer

Candidates should possess the following qualification:

B.Pharm | M.Pharm

Relevant experience in pharmaceutical manufacturing, particularly ointment manufacturing operations, would be applicable to this position.

Kamla Lifesciences Ointment Officer: Key Responsibilities

• Supervise and monitor ointment manufacturing activities.
• Ensure compliance with SOPs, GMP and quality standards.
• Maintain accurate records and documentation.
• Support process improvement and efficient production.

How to Apply

Interested candidates can send their updated CV to the following email address:

Email: anjali.yadav@kamlagroup.co.in
Contact: 8956480712

Candidates should include their relevant qualification and pharmaceutical manufacturing experience in the updated resume.

Job Summary

Shri Laxmi Chem Pharma Pvt. Ltd. is hiring Chemists / Senior Chemists for its Quality Control Department.
There are 2 positions available for candidates with B.Sc. or M.Sc. in Chemistry.
The role requires 1–4 years of experience in pharmaceutical quality control and laboratory activities.
Candidates with knowledge of GC, HPLC, GMP, GLP and laboratory documentation can apply for the opportunity at Chhatral.

Shri Laxmi Chem Pharma Quality Control: Chemist / Sr. Chemist

Shri Laxmi Chem Pharma QC: Job Details

Designation: Chemist / Sr. Chemist – Quality Control
Department: Quality Control
No. of Positions: 02
Location: Chhatral
Experience: 1–4 Years

Shri Laxmi Chem Pharma QC: Eligibility & Qualifications

Candidates should have a qualification in Chemistry:

B.Sc. Chemistry | M.Sc. Chemistry

Relevant experience in pharmaceutical quality control and laboratory analysis will be considered for the position.

Shri Laxmi Chem Pharma QC: Desired Skills

• Knowledge of GC, HPLC and other laboratory instruments.
• Understanding of GMP, GLP and SOPs.
• Good documentation and data integrity practices.
• Good communication and teamwork skills.
• Ability to follow approved specifications and standard operating procedures.
• Knowledge of laboratory testing and analytical documentation.

Shri Laxmi Chem Pharma QC: Key Responsibilities

Laboratory Testing & Instrument Handling

• Operate and maintain laboratory instruments such as GC, HPLC and other equipment.
• Ensure testing is performed as per approved specifications and SOPs.
• Maintain laboratory instruments and support routine analytical activities.

Quality Control Documentation

• Maintain accurate laboratory records and analytical documentation.
• Ensure proper documentation and data integrity practices.
• Investigate OOS/OOT results and support corrective actions.
• Ensure compliance with GMP, GLP, SOPs and safety requirements.

How to Apply

Interested candidates can apply for the Chemist / Sr. Chemist – Quality Control position by submitting their updated resume.

Apply through:
Shri Laxmi Chem website

Email: hr@dhruvumediess.com

Job Summary

Amneal Pharmaceuticals is hiring freshers for the Quality Control (OSD) Department at its SEZ facility in Matoda, Ahmedabad.
The position is for an Apprentice role in pharmaceutical quality control and is suitable for candidates with a B.Sc. or M.Sc. in Chemistry.
Selected candidates will gain practical exposure to pharmaceutical QC testing, analytical instruments, laboratory documentation and GMP requirements.
Candidates interested in building a career in Pharmaceutical Quality Control can apply by sharing their updated resume with the recruitment team.

Amneal Pharmaceuticals Quality Control OSD Apprentice

Amneal Pharmaceuticals QC OSD: Job Details

Company: Amneal Pharmaceuticals
Department: Quality Control – OSD
Designation: Apprentice
Location: SEZ, Matoda, Ahmedabad
Experience: Fresher
Candidate Preference: Local candidates preferred; male candidates preferred.

Amneal Pharmaceuticals QC OSD: Eligibility & Qualifications

Candidates with the following qualifications are eligible:

B.Sc. Chemistry | M.Sc. Chemistry | B.Sc. Analytical Chemistry | M.Sc. Analytical Chemistry | Relevant Chemistry Qualification

Freshers with academic projects, internships or industrial training exposure in pharmaceutical quality control may be preferred.

Amneal Pharmaceuticals QC OSD: Desired Profile

• Basic understanding of pharmaceutical quality control and analytical chemistry.
• Basic knowledge of cGMP, GLP and ALCOA/ALCOA+ principles.
• Basic knowledge of analytical instruments such as HPLC, UPLC, GC, UV and IR will be an advantage.
• Good communication and interpersonal skills.
• Basic computer knowledge and willingness to learn laboratory software and documentation systems.
• Strong attention to detail with a commitment to data integrity and quality.
• Willingness to work in a regulated GMP environment.
• Candidates interested in developing a career in pharmaceutical quality control are encouraged to apply.

Amneal Pharmaceuticals QC OSD: Key Responsibilities

Quality Control Testing

• Perform routine analysis of raw materials, in-process samples and finished products under the guidance of senior QC personnel.
• Gain hands-on exposure to HPLC, UPLC, GC, UV, IR and other analytical instruments.
• Perform QC testing of topical, gel, solution, cream and other pharmaceutical products.
• Support sampling, testing, calibration and routine laboratory activities.

Amneal Pharmaceuticals QC Documentation & Compliance

• Follow SOPs, cGMP, GLP and ALCOA/ALCOA+ principles.
• Maintain accurate laboratory records, worksheets, logbooks and analytical documentation.
• Ensure compliance with applicable quality and regulatory requirements.
• Maintain laboratory safety, cleanliness and housekeeping standards.
• Collaborate effectively with QC and cross-functional teams.

How to Apply

Interested candidates can share their updated resume with the Amneal Pharmaceuticals recruitment team.

Email:
PriyaR.Sharma@amneal.com
Khushi.Acharya@amneal.com

Candidates should mention their relevant qualification and experience details in their resume while applying.

Job Summary

Dr. Reddy’s Laboratories is conducting a Career Expo for API Manufacturing and is hiring Team Members for its API Production operations.
The opportunity is open to candidates with Diploma or B.Sc. Chemistry qualifications and relevant experience in API manufacturing.
Selected candidates will work with API production equipment and manufacturing processes while following BMR/BPR, SOP, GMP and safety standards.
Candidates with 3 to 6 years of experience in API production can attend the Career Expo and apply for the available opportunity.

Dr. Reddy’s Laboratories Team Member – API Production

Dr. Reddy’s API Production: Position Details

Position: Team Member – API Production
Department: API Production
Job Location: Hyderabad
Experience: 3–6 Years
Qualification: Diploma or B.Sc. Chemistry

Dr. Reddy’s API Production: Eligibility & Qualifications

Candidates must have one of the following qualifications:

Diploma | B.Sc. Chemistry

Relevant experience in API production and pharmaceutical manufacturing is required.

Dr. Reddy’s API Production: Experience Required

Candidates should have 3 to 6 years of experience in API manufacturing operations.

Relevant hands-on experience with API production equipment and manufacturing activities is required.

Dr. Reddy’s API Production: Key Responsibilities

API Manufacturing Operations

• Hands-on experience in operating API production equipment such as Reactors, ANFD and VTD.
• Execute manufacturing activities according to BMR/BPR, SOPs, GMP and safety standards.
• Experience in manufacturing API products in accordance with batch production records and standard operating procedures.
• Follow established manufacturing processes and safety requirements during API production operations.

Dr. Reddy’s Laboratories Career Expo Details

Interview Date & Time

Date: 4 October 2026 (Sunday)
Time: 9:00 AM to 3:00 PM

Job Location

Dr. Reddy’s Laboratories Ltd., Leadership Academy
Bachupally, Hyderabad – 500090.

How to Apply

Interested candidates can apply by scanning the QR code provided in the recruitment notification.

Career Expo Application

Candidates meeting the qualification and experience requirements can attend the Career Expo and apply for the Team Member – API Production position.

Job Summary

Mylan Laboratories Limited, a Viatris company, is conducting a Recruitment Drive for Quality Control professionals.
The opening is for Officer / Executive positions supporting its OSD manufacturing operations.
Candidates with M.Sc Chemistry, B.Pharm or M.Pharm qualifications and 1 to 7 years of relevant experience can apply.
The recruitment drive will be conducted on 4 October 2026 in Vadodara, Gujarat.

Mylan Laboratories Quality Control Officer / Executive Recruitment

Mylan Laboratories Limited is hiring professionals for its Quality Control function associated with its OSD Manufacturing Facility at Pithampur, Indore.

Mylan Laboratories Quality Control: Position Details

Department: Quality Control
Position: Officer / Executive
Experience: 1–7 Years
Qualification: M.Sc Chemistry / B.Pharm / M.Pharm

Mylan Laboratories Quality Control: Eligibility & Qualifications

Eligible candidates can have any of the following qualifications:

M.Sc Chemistry | B.Pharm | M.Pharm

Candidates should have relevant experience in pharmaceutical Quality Control operations.

Mylan Laboratories Quality Control: Required Skills

Relevant experience includes:

• RM / PM / Stability / FG analysis.
• Method Transfer and laboratory investigation activities.
• Hands-on experience with HPLC, GC, Dissolution and other instrumental analysis.
• Experience with LIMS and laboratory software.
• Knowledge of pharmaceutical Quality Control laboratory operations.

Mylan Laboratories Quality Control Recruitment: Experience

The position requires 1 to 7 years of experience in relevant Quality Control activities.

Candidates with experience in pharmaceutical analytical testing, instrumental analysis, stability testing, method transfer and laboratory investigations can apply.

Mylan Laboratories Recruitment Drive Details

Interview Date & Time

Date: 4 October 2026
Time: 10:00 AM to 5:00 PM

Interview Venue

Hotel Suba Elite
Abbas Tyabji Road,
Next to Parsi Agiyari,
Jayesh Colony, Fatehgunj,
Vadodara, Gujarat.

How to Apply

Eligible candidates interested in the Quality Control Officer / Executive opportunity can attend the recruitment drive at the mentioned venue with their updated resume and relevant documents.

Candidates should ensure that their qualifications and experience match the requirements before attending the drive.

Job Summary

Torrent Pharmaceuticals is conducting a Walk-In Interview for the position of Executive – Bioanalytical at its R&D Centre.
The opportunity is open to candidates with M.Pharm or M.Sc qualifications and 3 to 8 years of relevant experience.
The role involves bioanalytical method development, validation, sample analysis, laboratory instrument operation and regulatory compliance.
Eligible candidates can attend the walk-in interview on 4 October 2026 at the Torrent Pharmaceuticals R&D Centre.

Torrent Pharmaceuticals Executive – Bioanalytical Recruitment

Torrent Pharmaceuticals Bioanalytical Department

Position: Executive – Bioanalytical
Department: Bioanalytical
Experience: 3–8 Years
Qualification: M.Pharm / M.Sc
Job Location: R&D Centre, Gandhinagar, Gujarat

Torrent Pharmaceuticals Executive – Bioanalytical: Eligibility & Qualifications

Candidates with the following qualifications are eligible:

M.Pharm | M.Sc

Relevant experience in bioanalytical laboratory operations is required.

Torrent Pharmaceuticals Executive – Bioanalytical: Key Responsibilities

• Develop and validate sensitive and rugged bioanalytical methods using different extraction techniques such as SPE and LLE.
• Perform quantitation using techniques including LCMS and HPLC for analysis of drug substances.
• Conduct sample analysis for Bioavailability/Bioequivalence studies independently with the required accuracy.
• Operate, maintain and calibrate laboratory instruments according to written instrument operating procedures.
• Maintain GDP and GLP compliance in the laboratory.
• Maintain knowledge of current applicable regulatory requirements.

Torrent Pharmaceuticals Executive – Bioanalytical: Required Experience

Candidates should have 3 to 8 years of relevant experience in bioanalytical activities, including method development, method validation, sample analysis and laboratory instrument operations.

Torrent Pharmaceuticals Walk-In Interview Details

Interview Date & Time

Date: 4 October 2026 (Sunday)
Time: 10:00 AM to 03:00 PM

Interview Venue

Torrent Pharmaceuticals Ltd. R&D Centre
Ahmedabad Airport Gandhinagar Highway,
Besides Amul Mother Dairy & Kanoria Hospitals,
Near Indira Bridge, Village: Bhat,
Gandhinagar – 382428.

Important Note

Candidates who have attended an interview during the last 6 months need not apply.

How to Apply

Interested candidates can attend the walk-in interview with their updated resume.

Candidates can also share their resume through email:

meghamaheshwari@torrentpharma.com
vilshashah@torrentpharma.com

Job Summary

Amneal Pharmaceuticals is hiring candidates for Manufacturing & Packing and Quality Control functions at its regulated pharmaceutical plant in SEZ Matoda, Ahmedabad.
The openings are available for candidates with relevant experience in OSD manufacturing, packing and pharmaceutical quality control.
Candidates with B.Pharm, B.Sc, M.Sc, Diploma, ITI or BA qualifications can apply for the respective positions.
The required experience for both openings is 2 to 7 years, with relevant pharmaceutical industry experience preferred.

Amneal Pharmaceuticals Manufacturing & Packing Jobs

Manufacturing & Packing – Operator to Executive

Designation: Operator to Executive
Experience: 2–7 Years
Job Location: SEZ Matoda, Ahmedabad

Amneal Pharmaceuticals Manufacturing & Packing: Eligibility & Qualifications

Eligible qualifications include:

B.Pharm | B.Sc | Diploma | ITI | BA

Amneal Pharmaceuticals Manufacturing & Packing: Required Skills

• Experience in Granulation, Coating, Compression and Bottle Packing Capsules.
• Machine exposure to RM/EBE, FETTE, Autocoaters and bottle packing lines.
• Experience with track and trace systems.

Amneal Pharmaceuticals Quality Control Jobs

Quality Control – Officer to Executive

Designation: Officer to Executive
Experience: 2–7 Years
Job Location: SEZ Matoda, Ahmedabad

Amneal Pharmaceuticals Quality Control: Eligibility & Qualifications

Eligible qualifications include:

M.Sc | B.Sc | B.Pharm

Amneal Pharmaceuticals Quality Control: Required Skills & Responsibilities

• Perform analysis of raw materials, in-process materials and finished products.
• Hands-on experience with UV, IR, HPLC, UPLC, GC and LCMS.
• Knowledge of cGMP and 21 CFR requirements.
• Knowledge of ALCOA++ and LIMS.
• Experience in analysis of IP/FP/PM/VM/MT and stability samples.
• Experience operating QC instruments, including HPLC, UV, Dissolution, GC and PSD.

Amneal Pharmaceuticals Manufacturing & Quality Control: Job Location

The available opportunities are based at the SEZ Matoda pharmaceutical manufacturing facility in Ahmedabad.

Eligibility & Qualifications

Candidates with relevant pharmaceutical manufacturing or quality control experience can apply for the respective roles.

B.Pharm | B.Sc | M.Sc | Diploma | ITI | BA

Relevant experience in OSD manufacturing, packing, pharmaceutical analysis and quality control is applicable according to the position.

How to Apply

Interested candidates can share their updated CV through the following email addresses:

• chandanid@amneal.com
• PriyaR.sharma@amneal.com
• Jyoti.Parmar@amneal.com

Candidates should mention the relevant department or position while submitting their resume.

Job Summary

InfiChem Pharma Private Limited is hiring experienced professionals for a Production Chemist/Officer position at its pharmaceutical manufacturing facility.
The opportunity is open to candidates with experience in API or Intermediate production operations.
Candidates with B.Sc or M.Sc Chemistry or an equivalent qualification can apply for this role.
The position requires a minimum of 3 years of relevant production experience, with a salary of up to ₹4.2 LPA.

InfiChem Pharma Production Chemist/Officer

InfiChem Pharma Private Limited is looking for experienced candidates to join its Production team at GIDC, Vapi.

InfiChem Pharma Production Chemist/Officer: Job Details

Position: Production Chemist/Officer
Company: InfiChem Pharma Private Limited
Location: GIDC, Vapi
Experience: Minimum 3 years
Salary: Up to ₹4.2 LPA

InfiChem Pharma Production Chemist/Officer: Eligibility & Qualifications

Candidates should meet the following eligibility requirements:

B.Sc Chemistry | M.Sc Chemistry | Equivalent Qualification

Experience Required

• Minimum 3 years of experience in Production.
• Relevant experience in API or Intermediate production is required.

InfiChem Pharma Production Chemist/Officer: Key Requirements

• Experience in pharmaceutical production operations.
• Relevant experience in API or Intermediate manufacturing.
• Qualification in Chemistry or an equivalent discipline.

How to Apply

Interested candidates may send their updated resume to the recruitment team.

Email: hr@infichem.in
Contact: +91 7778862622 (WhatsApp Only)

Candidates with relevant Production experience can share their updated CV through the above contact details.

Job Summary