Pharma Jobs

GUFIC Walk In Interview Navsari GUFIC Walk In Interview Navsari is an excellent opportunity for freshers who want to start their career with a reputed pharmaceutical company. GUFIC Biosciences Ltd is conducting a walk-in interview on 24 January 2026 (Saturday) for its injectable and API manufacturing facility located at Navsari, Gujarat. This walk-in drive is strictly for freshers and offers roles in Quality Assurance and Production departments. Company Profile – GUFIC Biosciences Ltd GUFIC Biosciences Ltd has been serving the pharmaceutical industry since 1970 and is one of the leading companies in lyophilized injections. The company has a strong presence in regulated markets and holds approvals from WHO GMP, EU GMP, Canada, Russia, ANVIZA, Yemen, Uzbekistan, and more. Job Location Navsari, Gujarat Walk-In Interview Details Departments & Educational Qualification Quality Assurance (Injectable / API) Production (Injectable) Production (API) – Male Candidates Only Important Educational Requirement Candidates must carry original degree certificates issued by the educational institute or university. ⚠️ Provisional degree certificates will NOT be accepted. Documents to Carry Contact Details (If Unable to Attend Walk-In) Interested candidates can send their updated CV to: Walk-In Interview Venue GUFIC Biosciences LtdN.H. 48, Near GEB Grid,Kabilpore, Navsari – 396445,Gujarat, India

Glenmark Walk In Drive Chhatrapati Sambhajinagar Glenmark Walk In Drive Chhatrapati Sambhajinagar is a great opportunity for experienced pharmaceutical professionals looking to build a strong career in Quality Control and Quality Assurance. Glenmark Pharmaceuticals Limited is conducting a walk-in interview on 24th January 2026 (Saturday) at its Chhatrapati Sambhajinagar (Aurangabad), Maharashtra facility. Candidates with hands-on experience in sterile, liquid, spray, ointment, and inhalation dosage forms are encouraged to attend this walk-in interview. Company Name Glenmark Pharmaceuticals Limited Glenmark is a globally recognized pharmaceutical company known for its strong presence in regulated markets and high-quality manufacturing standards. Glenmark Walk In Drive Chhatrapati Sambhajinagar Job Location Chhatrapati Sambhajinagar (Aurangabad), Maharashtra Department Job Designation Educational Qualification Candidates must have one of the following qualifications: Note: Education criteria is mandatory as per Glenmark guidelines. Work Experience Required Candidates not matching the experience criteria are advised not to attend the walk-in interview. Job Profile & Responsibilities Quality Control (QC): Quality Assurance (QA): Walk-In Interview Details Interview Venue Glenmark Pharmaceuticals LimitedPlot No. B-25, Shendra MIDC,Chhatrapati Sambhajinagar (Aurangabad) – 431154,Maharashtra, India Documents to Carry Interested candidates must carry: Unable to Attend Walk-In? Candidates who are unable to attend the walk-in interview may send their CV to the official email ID: aurangabad.reception@glenmarkpharma.com

Regulatory Affairs Job in Ahmedabad Noronic Pharmaceutical Private Limited is hiring experienced Regulatory Affairs professionals to join its growing pharmaceutical team. This is an excellent opportunity for candidates with OSD regulatory experience looking for a stable and growth-oriented career in Ahmedabad, Gujarat. Company Details Regulatory Affairs Job in Ahmedabad Open Positions Noronic Pharmaceutical is hiring for the following roles: Qualification & Experience Experience Required: Educational Qualification: Key Responsibilities – Regulatory Affairs Candidate Preference Job Location How to Apply Interested and eligible candidates can apply by sending their updated CV to the HR email ID below: 📩 Email: hr@noronicpharma.com

QC In Charge Job Vacancy QC In Charge Job Vacancy has been announced by InfiChem Pharma Private Limited, Vapi, for experienced professionals in API / Pharmaceutical Manufacturing. This is an excellent opportunity for candidates with strong HPLC and GC expertise who want to build and lead a Quality Control department from the ground up. Company Details InfiChem Pharma is developing a modern API manufacturing facility and is looking for a skilled Quality Control leader to ensure compliance, quality systems, and laboratory readiness. Job Details This QC In Charge Job Vacancy is ideal for professionals who have hands-on exposure to analytical instruments and experience setting up QC operations. Job Summary The selected candidate will be responsible for establishing and managing the Quality Control function for a new API manufacturing unit. This includes laboratory setup, documentation, systems implementation, and regulatory compliance. Key Responsibilities Required Skills & Qualifications Job Location Candidates willing to work at a developing API manufacturing facility will be preferred. How to Apply Interested candidates can send their updated resume to: Email: hr@infichem.in WhatsApp: +91 77788 62622 Mention “QC In Charge – Vapi” in the subject line for faster processing.

Executive Quality Control Job in Gandhidham 2026 Are you looking for an Executive Quality Control job in Gandhidham in the pharmaceutical API sector? Rusan Pharma Limited is hiring experienced professionals for its Quality Control (API) department at Gandhidham (Kandla), Gujarat. This opportunity is ideal for candidates with strong analytical skills and hands-on experience in API quality control. Company Overview – Rusan Pharma Limited Rusan Pharma Limited is a well-established pharmaceutical company known for its expertise in API manufacturing and adherence to global quality and compliance standards. The company focuses on data integrity, cGMP compliance, and regulatory excellence. Job Details – Executive Quality Control Executive Quality Control Job in Gandhidham 2026 Role & Responsibilities As an Executive – Quality Control, the selected candidate will be responsible for: Executive Quality Control Job in Gandhidham 2026 Eligibility Criteria To apply for this role, candidates must have: Job Location – Gandhidham (Kandla), Gujarat The role is based in Gandhidham (Kandla), a major industrial and pharmaceutical hub in Gujarat, offering excellent career growth opportunities in API manufacturing. Executive Quality Control Job in Gandhidham 2026 How to Apply Interested and eligible candidates can share their updated CV via email: Email ID:sunil.namdev@rusanpharma.com Mention “Executive – Quality Control” in the subject line for faster processing. Job Summary Table Particulars Details Job Role Executive – Quality Control Company Rusan Pharma Limited Department Quality Control (API) Location Gandhidham, Gujarat Experience 4–6 Years Qualification M.Sc / B.Pharm

Quality Control Sr. Analyst Job in Hyderabad 2026 Are you an experienced analytical professional aiming for a Quality Control Sr. Analyst job in Hyderabad 2026? Ritsa Pharma Pvt. Ltd, a reputable pharmaceutical contract development and manufacturing organization based in Genome Valley, Hyderabad, is hiring for a Senior Quality Control Analyst position. This role focuses on analytical testing, compliance with regulatory standards, and ensuring quality systems in pharmaceutical manufacturing. About Ritsa Pharma Pvt. Ltd Ritsa Pharma Pvt. Ltd is a modern, growth-oriented pharmaceutical contract development and manufacturing organization (CDMO) specializing in solid oral dosage (tablets/capsules) production and related analytical services. The company emphasizes quality, compliance, and scientific excellence, with strong regulatory credentials and a culture focused on operational integrity. Job Overview – Quality Control Sr. Analyst Job in Hyderabad 2026 Quality Control Sr. Analyst Job in Hyderabad 2026 Key Responsibilities As a Quality Control Sr. Analyst, you will be responsible for: ✔ Performing both routine and non-routine analytical testing of raw materials, in-process, finished products, and stability samples.✔ Operating, calibrating, and troubleshooting analytical instruments including HPLC, UV, IR, and GC.✔ Preparing, reviewing, and validating analytical documents such as SOPs, Certificates of Analysis (COAs), and test reports.✔ Ensuring compliance with Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), and data integrity principles (like ALCOA+).✔ Maintaining laboratory documentation, handling deviations, OOS/OOT results, and supporting investigations.✔ Assisting in audit preparation and maintaining audit readiness.✔ Collaborating with cross-functional teams for timely batch and sample release. Quality Control Sr. Analyst Job in Hyderabad 2026 Required Qualifications & Skills ✔ Bachelor’s or Master’s degree in Chemistry, Pharmaceutical Sciences, or a related field.✔ Hands-on experience with analytical instruments (HPLC, UV, IR, GC) in a regulated environment.✔ Strong knowledge of GMP/GLP, data integrity (ALCOA+), and documentation standards.✔ Ability to handle analytical testing, troubleshoot instruments, and interpret results accurately.✔ Excellent communication and teamwork skills are advantageous. Job Location – Hyderabad, Telangana Located in Genome Valley, Hyderabad is one of India’s premier pharmaceutical and biotechnology hubs, offering modern infrastructure, regulatory-focused manufacturing units, and fast-growing career opportunities in the life sciences sector. Why Apply for This Job Joining Ritsa Pharma as a Quality Control Sr. Analyst helps you: ✔ Develop expertise in pharmaceutical analytical testing within a regulated environment.✔ Work with cutting-edge analytical technologies and compliance systems.✔ Strengthen your career profile in a growing CDMO with global regulatory exposure.✔ Be part of a team driving quality, integrity, and patient-focused results. Job Summary Table Job Role Quality Control Sr. Analyst Company Ritsa Pharma Pvt. Ltd Location Hyderabad, Telangana Function Quality Control / Quality Assurance Experience Mid-Senior Level Qualification Chemistry / Pharma / Science Industry Pharmaceutical Manufacturing

Senior Quality Control Analyst Job in Hyderabad 2026 Are you a skilled pharmaceutical professional looking for a Senior Quality Control Analyst job in Hyderabad 2026? Ritsa Pharma Pvt. Ltd, a growing pharmaceutical company, has opened applications for a Senior Quality Control Analyst position at its Hyderabad, Telangana facility. This role offers a strong opportunity to work in quality assurance within a regulated pharmaceutical environment. About Ritsa Pharma Pvt. Ltd Ritsa Pharma Pvt. Ltd is an emerging pharmaceutical manufacturing company focused on delivering high-quality healthcare products. The organization emphasizes analytical excellence, regulatory compliance, and strong quality systems to meet industry standards. Senior Quality Control Analyst Job in Hyderabad 2026 Job Details Senior Quality Control Analyst Job in Hyderabad 2026 Key Responsibilities As a Senior Quality Control Analyst, your core duties will include: Required Qualifications & Skills To succeed in this role, you should have: Job Location – Hyderabad, Telangana Working in Hyderabad gives you exposure to one of India’s fastest-growing pharmaceutical industries, with access to advanced labs, quality systems, and career growth opportunities. Why Apply for This Job Joining Ritsa Pharma as a Senior Quality Control Analyst means: ✔ Playing a key role in pharmaceutical quality assurance.✔ Working with modern analytical instruments.✔ Gaining experience in regulated manufacturing environments.✔ Contributing to product quality and compliance. Table Job Role Senior Quality Control Analyst Company Ritsa Pharma Pvt. Ltd Location Hyderabad, Telangana Function Quality Control / Quality Assurance Experience Mid-Senior Level Industry Pharmaceutical Manufacturing

Eris Therapeutics Apprentice Vacancy in Ahmedabad Eris Therapeutics Ltd., a leading pharmaceutical company, has announced a new Apprentice job vacancy for freshers and early-career candidates. The company is inviting applications for Apprentice positions in Production, Quality Control, and Quality Assurance departments at its Ahmedabad, Gujarat facility. This opportunity is ideal for candidates who want to start their pharmaceutical career with a reputed organization. Company Details Apprentice Departments Eris Therapeutics is hiring Apprentices for the following departments: Eligibility Criteria Educational Qualification: Candidates must have completed any of the following: Both freshers and eligible candidates can apply for this apprentice opportunity. Job Location How to Apply for Eris Therapeutics Apprentice Vacancy Interested candidates can send their updated CV to the official recruitment email: Email ID: recruitment@eristherapeutics.com Contact Details (For More Information)

Regulatory Affairs Internship in Pune Agenome Research has announced an excellent opportunity for freshers and early-career professionals through its Regulatory Affairs Internship Program in PCMC, Pune. The company is hiring 15 Regulatory Affairs Interns who are eager to gain real-world regulatory experience under expert guidance. This internship is ideal for pharmacy, medical, and life sciences graduates looking to build a strong foundation in Regulatory Affairs. Company Overview Internship Details Key Responsibilities – Regulatory Affairs Intern Eligibility Criteria Educational Qualification: Language Requirements: Desired Skills: Why Join Agenome Research? Selection Process How to Apply Interested candidates can apply online by filling out the application form: 🔗 Application Link:https://forms.gle/AYWhKfssmvisdMKL7 (You may also scan the QR code mentioned in the official poster)

Ceph Lifesciences Job Vacancy in Baddi Ceph Lifesciences, a reputed pharmaceutical company, has announced a new job vacancy in Baddi, Himachal Pradesh. The company is hiring experienced and qualified candidates across Production, QA, QC, Oral Manufacturing, and Microbiology departments. This is an excellent opportunity for pharma professionals looking to grow their careers in a GMP-compliant manufacturing facility. Company Details Available Job Vacancies at Ceph Lifesciences Production Injection (Dry Powder Injection) Position Qualification Experience Vacancies Operator / Senior Operator (Filling) 10+2 / ITI 3–10 Years 4 Officer – Manufacturing B.Pharm / M.Pharm 1–3 Years 4 Operator (Sealing) 10+2 / ITI 2–5 Years 1 Executive / Sr. Executive – QMS B.Pharm / M.Pharm 5–9 Years 1 Data Entry Operator Graduation (Diploma in Computer) 1–3 Years 1 Production Oral Department Position Qualification Experience Vacancies QMS Officer B.Pharm 2–5 Years 1 Manufacturing Officer B.Pharm 1–3 Years 2 BQS Operator 10+2 / ITI 3–5 Years 1 Quality Assurance (QA) Department Position Qualification Experience Vacancies Validation – Sr. Officer / Sr. Executive (Injection) B.Pharm 3–10 Years 2 Validation Officer / Sr. Officer (Oral) B.Pharm 1–4 Years 1 QA QMS Officer / Sr. Officer B.Pharm / M.Pharm 2–4 Years 3 QA QMS / Document Review – Assistant Manager B.Pharm / M.Pharm 8–10 Years 1 IPQA Officer (Oral) B.Pharm 1–4 Years 1 Quality Control (QC) Department Position Qualification Experience Vacancies Officer – HPLC B.Pharm / M.Sc 1–3 Years 3 Executive / Sr. Executive – RM B.Pharm / M.Sc 4–9 Years 1 Microbiology Department Position Qualification Experience Vacancies Microbiologist M.Sc / B.Tech (Biotech – Micro) 1–2 Years 5 Walk-In Interview Details Documents Required: Contact Email HR Email ID: hr.unit6@neclife.com