vaibhav

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

Hy-Gro Chemicals Walk In Interview 2026 Hy-Gro Chemicals Walk In Interview 2026 has been announced for multiple departments at its IDA Bollaram, Telangana facility. Hy-Gro Chemicals Pharmtek Pvt. Ltd., a leading bulk drugs and APIs manufacturer, is inviting experienced and immediate joiner candidates for QC, QA, Production, and EHS departments. About Hy-Gro Chemicals Pharmtek Pvt. Ltd. Hy-Gro Chemicals Pharmtek Pvt. Ltd. is a reputed Bulk Drugs & APIs manufacturer, certified by USFDA, KFDA, EDQM, and ANVISA (Brazil). The company is known for its strong regulatory compliance and quality manufacturing practices. Walk-In Interview Schedule Department-Wise Job Vacancies 🔹 Quality Control (QC) Production EHS Quality Assurance (QA) Eligibility Criteria Candidates applying for Hy-Gro Chemicals Walk In Interview 2026 must meet the following conditions: Documents Required Candidates must carry the following documents: Interview Venue Hy-Gro Chemicals Pharmtek Pvt. Ltd. (Unit-I)Plot No: 174, Progressive Industrial Society,IDA – Bollaram, Jinnaram (M),Sangareddy (D) – 502325, Telangana Unable to Attend Walk-In? Candidates who are unable to attend the interview can send their profiles to: hr@hygrochemicals.com Mention your Department name in the email subject Why Apply for Hy-Gro Chemicals Walk In Interview 2026? Job Summary Table Company Hy-Gro Chemicals Pharmtek Pvt. Ltd. Interview Type Walk-In Departments QC, QA, Production, EHS Qualification B.Sc, M.Sc Experience 0 – 5 Years Job Location IDA Bollaram, Telangana Interview Dates 19–24 January 2026

Otsuka Pharma Walk In Interview 2026 Otsuka Pharma Walk In Interview 2026 has been officially announced by Otsuka Pharmaceutical India Private Limited (OPI) for experienced professionals in Quality Control (QC) and Quality Assurance (QA) departments. The walk-in interview will be conducted on 24 January 2026 (Saturday) in Ahmedabad, Gujarat for candidates with experience in parenteral and injectable formulations. About Otsuka Pharmaceutical India Pvt. Ltd. Otsuka Pharmaceutical India Private Limited is a global healthcare company primarily engaged in manufacturing IV fluids and parenteral nutrition products. The company serves multiple therapeutic segments and markets worldwide and is known for its high standards of quality, compliance, and innovation. Walk-In Interview Details Department-Wise Job Openings Quality Control (QC) Functions: IPPT, FP, RM, PM, Stability, Micro Quality Assurance (QA) Functions: Equipment Qualification, Validation, QMS Eligibility & Important Notes Candidates applying for Otsuka Pharma Walk In Interview 2026 should note the following: Documents to Carry Freshers may email their CV to:hrm.opmf-amd@otsukapharma.in Interview Venue Otsuka Pharmaceutical India Pvt. Ltd.21st Floor, B-Block, Westgate,Nr. YMCA, S.G. Highway,Ahmedabad – 380015 Important Notice Otsuka Pharmaceutical India Pvt. Ltd. does not charge any fees for interviews or job offers. Beware of fraudulent calls or consultants asking for money. Why Attend Otsuka Pharma Walk In Interview 2026? Job Summary Table Company Otsuka Pharmaceutical India Pvt. Ltd. Interview Type Walk-in Departments Quality Control, Quality Assurance Experience 2 – 6 Years Qualification B.Sc, M.Sc, B.Pharm, M.Pharm Location Ahmedabad, Gujarat

Aurobindo Pharma Virtual Interview 2026 Aurobindo Pharma Virtual Interview 2026 has been officially announced for experienced candidates in Production and Packing departments. Aurobindo Pharma Limited is conducting virtual interviews for its APL Health Care Limited – Unit IV, located at Naidupeta, Tirupati District, Andhra Pradesh. This is an excellent opportunity to join one of India’s leading pharmaceutical companies. About Aurobindo Pharma Aurobindo Pharma is a globally recognized pharmaceutical company with a strong presence in generic medicines and active pharmaceutical ingredients (APIs). The company offers excellent career growth, world-class manufacturing facilities, and a professional work culture. Interview Type & Work Location Department-Wise Job Openings Production Department OSD (Granulation, Compression, Coating, Capsule Filling) Oral Liquid & Nasal Spray Packing Department OSD (Blister & Bottle) Eligibility Criteria Candidates applying for Aurobindo Pharma Virtual Interview 2026 should have: Registration Process Interested candidates must scan the QR code provided in the notification to register for the virtual interview and complete the application process. Contact Details For any queries regarding the interview: Why Join Aurobindo Pharma? Summary Table Company Aurobindo Pharma Interview Mode Virtual Departments Production, Packing Experience 2 – 8 Years Qualification ITI, Diploma, Degree, B.Pharm, M.Pharm Location Naidupeta, Andhra Pradesh

Bharat Biotech Walk In Interview 2026 Bharat Biotech Walk In Interview 2026 has been officially announced for experienced candidates in Injectable and Vaccine Manufacturing. Bharat Biotech International Limited is conducting a walk-in interview on 25th January 2026 (Sunday) at its Genome Valley facility, Hyderabad. This is a golden opportunity for skilled professionals to join one of India’s leading biotechnology companies. About Bharat Biotech International Limited Bharat Biotech is a globally recognized biotechnology company known for innovation in vaccines and biopharmaceuticals. With a strong presence in Genome Valley, Hyderabad, the company focuses on research, manufacturing, and development of life-saving vaccines and biologics. Walk-In Interview Details Qualification Required Candidates applying for Bharat Biotech Walk In Interview 2026 must have one of the following qualifications: Experience Required Hiring Department – Production Drug Substance (Bioprocess) Drug Product (Formulation & Filling) Documents Required for Interview Candidates must carry the following documents: Interview Venue Bharat Biotech International LimitedGenome Valley, Turkapally,Shamirpet, Hyderabad, Telangana Candidates can scan the QR code given in the notification for exact location. Why Attend Bharat Biotech Walk In Interview 2026? Summary Table Company Bharat Biotech Interview Type Walk In Date 25 January 2026 Experience 3–10 Years Department Production Location Hyderabad

Sai Life Sciences Formulation Development Job 2026 Sai Life Sciences, one of India’s fastest growing Contract Research, Development & Manufacturing Organisations (CRDMO), has announced an exciting Formulation Development (Preclinical) job opportunity for 2026. This role is based in Shameerpet, Hyderabad, Telangana, India, and is ideal for candidates with relevant scientific experience in preclinical formulation work. Sai Life Sciences is a globally recognized pharmaceutical company working with more than 300 innovator pharma and biotech partners to accelerate drug discovery and development across small molecule programs. About Sai Life Sciences Sai Life Sciences is a leading CRDMO supporting global pharma innovation with capabilities spanning discovery chemistry, process development, analytical sciences, formulation research, and manufacturing. The company fosters a culture of scientific excellence, transparency, and inclusive growth, and has been certified as a Great Place To Work, reflecting its positive work environment. Job Overview – Formulation Development (Preclinical) Sai Life Sciences Formulation Development job 2026 Key Responsibilities A successful candidate for the Sai Life Sciences Formulation Development job 2026 will be responsible for:✔ Designing and executing pre-formulation experiments — including solubility, dissolution, particle characterization and excipient compatibility.✔ Supporting preclinical formulation strategies to assist lead identification and optimization.✔ Handling solid state assessment equipment like PXRD, DSC, TG, and particle analyzers.✔ Interpreting and documenting scientific data with high accuracy.✔ Maintaining good laboratory practices, ELN documentation, and compliance with safety/chemical risk standards. Sai Life Sciences Formulation Development job 2026 Required Qualifications & Skills To qualify for this role, candidates should have:✔ M.Sc / M.Pharm / M.Tech degree in Pharmaceutical Sciences, Chemical Sciences, or related discipline.✔ 1–3 years (or more) of hands-on experience in preclinical formulation development.✔ Strong knowledge of formulation principles and pre-formulation studies.✔ Experience with laboratory instruments like HPLC, GC, dissolution apparatus beneficial.✔ Good scientific documentation and communication skills. Sai Life Sciences Formulation Development job 2026 Location Benefits – Hyderabad Hyderabad is one of India’s major pharmaceutical and biotech hubs, offering strong R&D ecosystems, modern infrastructure, and excellent quality of life. Professionals in pharma research and formulation roles can expect fast career growth and opportunities to work on innovative drug development projects. Why Join Sai Life Sciences? Sai Life Sciences is committed to scientific excellence and employee growth. Working here provides: How to Apply Interested candidates should apply online via the Sai Life Sciences career portal (Darwinbox) and prepare for an interview-based selection process. Ensure your resume highlights your formulation experience and scientific achievements. Summary Table – Job Snapshot Job Title Sai Life Sciences Formulation Development (Preclinical) Location Shameerpet, Hyderabad, Telangana, India Experience 1–3 Years Qualification M.Sc / M.Pharm / M.Tech Department Formulation / Preclinical R&D Application Apply Online / Interview