Ceph Hiring QA, QC, Production & Engineering
- Company Overview
- Job Role & Responsibilities
- Production – Injection (Dry Powder Injection)
- Production – Oral Manufacturing
- Quality Assurance (QA) Department
- QA QMS / Document Reviewer – Deputy Manager
- QA QMS / Document Review – Assistant Manager
- IPQA Officer – Oral
- Quality Control (QC) Department
- Officer – HPLC
- Executive / Sr. Executive – QC Reviewer
- Microbiology Department
- Microbiologist
- Engineering Department
- Engineering QMS – Officer
- Process Maintenance – Executive
- Instrumentation Technician
- HVAC Technician
- Sealer Operator (Clean Room Class A)
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Why Consider a Career in Pharmaceutical Manufacturing?
- Frequently Asked Questions (FAQs)
- Job Summary
BPharm QA QC Production Jobs Baddi
B.Pharm/M.Pharm QA, QC, Production & Engineering vacancies at Ceph Lifesciences Baddi. Multiple roles with 1–13 yrs experience.
Ceph Lifesciences is expanding its manufacturing and quality teams at its Baddi facility in Himachal Pradesh and has announced multiple openings across Production, Quality Assurance, Quality Control, Microbiology, and Engineering departments. Professionals with experience in sterile injectable manufacturing, oral dosage production, QC HPLC analysis, and pharmaceutical engineering operations are invited to apply.
For candidates searching for pharma jobs in Baddi, QA QMS document reviewer roles, HPLC analyst vacancy in pharmaceutical companies, injectable production operator jobs, or pharmaceutical engineering maintenance careers, this hiring opportunity offers long‑term growth within a regulated manufacturing facility.
Company Overview
Ceph Lifesciences is a pharmaceutical manufacturing company based in Baddi, Himachal Pradesh—one of India’s largest pharmaceutical production clusters. The company specializes in formulation manufacturing including dry powder injections and oral dosage forms.
Operating under strict GMP-compliant systems, the facility focuses on high‑quality pharmaceutical manufacturing, regulatory documentation, and export‑grade product standards. Teams at Ceph work across formulation production, microbiology testing, analytical quality control, and engineering maintenance to ensure reliable and safe medicine manufacturing.
Working in such an environment provides exposure to:
- Sterile injectable manufacturing operations
- Oral solid dosage formulation production
- GMP and QMS compliance systems
- Analytical testing using HPLC and microbiological methods
- Pharmaceutical plant engineering and instrumentation systems
These roles directly support the safe production and quality assurance of medicines supplied to domestic and international healthcare markets.
Job Role & Responsibilities
Production – Injection (Dry Powder Injection)
Position: Operator / Senior Operator (Filling)
Qualification: 10+2 / ITI
Experience: 3–10 Years
Vacancies: 2
Responsibilities:
- Operate sterile filling equipment for dry powder injection manufacturing
- Follow aseptic manufacturing procedures and GMP guidelines
- Perform line clearance and equipment cleaning activities
- Maintain batch manufacturing documentation
- Ensure contamination control and sterile process compliance
Production – Oral Manufacturing
Position: Officer – Manufacturing
Qualification: B.Pharm / M.Pharm
Experience: 1–3 Years
Vacancies: 2
Position: Assistant Manager – Production Oral
Qualification: B.Pharm / M.Pharm
Experience: 8–13 Years
Vacancies: 1
Responsibilities:
- Supervise oral formulation manufacturing processes
- Ensure batch manufacturing record (BMR) compliance
- Manage production planning and manpower allocation
- Coordinate with QA/QC for in‑process quality checks
- Maintain regulatory compliance during manufacturing operations
Quality Assurance (QA) Department
QA QMS / Document Reviewer – Deputy Manager
Qualification: B.Pharm / M.Pharm
Experience: 10–13 Years
Vacancy: 1
Responsibilities:
- Review quality management system documentation
- Ensure regulatory compliance and data integrity
- Manage change control, deviations, and CAPA systems
- Support internal and external regulatory audits
QA QMS / Document Review – Assistant Manager
Qualification: B.Pharm / M.Pharm
Experience: 8–10 Years
Vacancy: 1
Responsibilities:
- Review batch records and GMP documentation
- Maintain QMS documentation systems
- Support audit readiness and compliance programs
IPQA Officer – Oral
Qualification: B.Pharm / M.Pharm
Experience: 1–3 Years
Vacancies: 2
Responsibilities:
- Perform in‑process quality checks during manufacturing
- Ensure GMP compliance during production activities
- Monitor process parameters and batch documentation
Quality Control (QC) Department
Officer – HPLC
Qualification: B.Pharm / M.Sc
Experience: 1–3 Years
Vacancies: 3
Responsibilities:
- Perform analytical testing using HPLC instruments
- Maintain laboratory documentation and calibration records
- Conduct stability and routine testing as per SOPs
- Support OOS investigations and data review
Executive / Sr. Executive – QC Reviewer
Qualification: B.Pharm / M.Sc
Experience: 5–8 Years
Vacancy: 1
Responsibilities:
- Review analytical data and chromatograms
- Verify laboratory reports and ensure GMP compliance
- Support regulatory audits and documentation review
Microbiology Department
Microbiologist
Qualification: M.Sc / B.Tech Biotechnology
Experience: 2–4 Years
Vacancy: 1
Responsibilities:
- Conduct microbiological testing of pharmaceutical products
- Perform environmental monitoring and sterility testing
- Maintain microbiology laboratory documentation
Engineering Department
Engineering QMS – Officer
Qualification: B.Tech
Experience: 1–2 Years
Vacancy: 1
Process Maintenance – Executive
Qualification: B.Tech
Experience: 5–8 Years
Vacancy: 1
Instrumentation Technician
Qualification: ITI / Diploma
Experience: 2–3 Years
Vacancy: 1
HVAC Technician
Qualification: 10+2 / ITI
Experience: 1–4 Years
Vacancy: 1
Sealer Operator (Clean Room Class A)
Qualification: 10+2 / ITI
Experience: 3–7 Years
Vacancies: 2
Responsibilities include maintaining pharmaceutical plant equipment, HVAC systems, instrumentation calibration, and ensuring proper functioning of cleanroom production environments.
Eligibility / Qualifications
Relevant Courses (comma‑separated):
B.Pharm, M.Pharm, B.Sc Chemistry, M.Sc Microbiology, M.Sc Biotechnology, B.Tech Biotechnology, B.Tech Mechanical, B.Tech Electrical, ITI Fitter, ITI Electrical, Diploma Mechanical Engineering, Diploma Instrumentation
Experience Range:
1–13 Years depending on role and department.
Industry Preference:
Candidates with pharmaceutical formulation manufacturing experience, sterile injectable exposure, analytical laboratory knowledge, or pharmaceutical engineering experience will be preferred.
Location & Salary
Location: Baddi, Himachal Pradesh
Industry: Pharmaceutical Formulation Manufacturing
Baddi is one of India’s largest pharmaceutical manufacturing hubs, hosting several major pharma companies and offering strong career opportunities in production, quality, and engineering domains.
Salary: As per industry standards based on role, experience, and technical expertise.
Application Process
Interested candidates can attend interviews from Monday to Saturday between 09:00 AM and 01:00 PM at the company facility.
Candidates should bring the following documents:
- Updated Resume
- Educational Certificates
- Experience Certificates
- Last Salary Slips
Interview Address:
Village Bhatole Kalan
Adjoining Jhair Mairl
Baddi, Himachal Pradesh – 174103
Why Consider a Career in Pharmaceutical Manufacturing?
Pharmaceutical manufacturing careers offer:
- Stable long‑term industry demand
- Global regulatory exposure (GMP compliance)
- Opportunities in production, quality, and engineering leadership
- Competitive salary growth in regulated pharma environments
Professionals experienced in sterile injectables, analytical QC testing, or pharmaceutical plant engineering are particularly valued in India’s expanding pharmaceutical export industry.
Frequently Asked Questions (FAQs)
1. What departments are hiring?
Production, Quality Assurance, Quality Control, Microbiology, and Engineering.
2. Are multiple experience levels accepted?
Yes, roles are available for candidates with 1–13 years of experience.
3. Is pharmaceutical experience required?
Yes, candidates with pharma formulation or manufacturing experience are preferred.
4. What analytical instruments are required for QC roles?
Hands‑on experience with HPLC and analytical laboratory systems.
5. Where is the job location?
Baddi, Himachal Pradesh – a major pharmaceutical manufacturing hub.
Job Summary
| Company | Ceph Lifesciences |
|---|---|
| Vacancies | Production Operator, Production Officer, QA QMS Reviewer, IPQA Officer, QC HPLC Officer, Microbiologist, Engineering Roles |
| Required Education | B.Pharm, M.Pharm, B.Sc, M.Sc, B.Tech, ITI, Diploma |
| Experience | 1–13 Years (Role Dependent) |
