1 Opening(s)
2.0 Year(s) To 3.0 Year(s)
3.00 LPA TO 4.20 LPA
Position: RA Officer
Location: Amedabad
Experience: 2 - 3 Years
Industries: Pharma
Responsibilities:
Prepare, review, and submit regulatory documents for the approval of drugs and pharmaceutical products.
Act as the main Coordinator between the company and Pharma Mfg company (like CDSCO, FDA, EMA).
Ensure compliance with all applicable ...
4 Opening(s)
2.0 Year(s) To 4.0 Year(s)
Not Disclosed by Recruiter
Candidate must have experience from Pharmaceutical Industry and should be ready for traveling for site work across Gujarat and India also.
Execute CSV activities as per GAMP 5, 21 CFR Part 11, and EU Annex 11
Prepare and execute validation deliverables:
Validation Plan / VMP sections
URS, FS, DS
Risk Assessments (FMEA / Risk-based)
IQ, OQ, ...
3 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.50 LPA TO 4.00 LPA
The Quality Assurance professional is responsible for ensuring that pharmaceutical products are manufactured, tested, and released in compliance with GMP and regulatory requirements. The role focuses on documentation, compliance, audits, and continuous quality improvement.
Roles and Responsibilities
GMP & Compliance
Ensure compliance with GMP, GDP, GLP, and regulatory guidelines
Review and approve SOPs, BMRs, ...
2 Opening(s)
3.0 Year(s) To 7.0 Year(s)
Not Disclosed by Recruiter
Key Responsibilities:
Brand Strategy
Market Research & Analysis
Project Management
Exposure to Omnichannel marketing
Stakeholder Management
Campaign & Promotion
Qualifications:
Bachelor’s degree in pharmacy, Life Sciences, or related field with MBA in Marketing or Healthcare Management.
3–4 years of experience in pharmaceutical marketing, preferably in ENT, Derma, or Critical Care, etc
Excellent communication, stakeholder management, and project management skills.
1 Opening(s)
2.0 Year(s) To 3.0 Year(s)
2.00 LPA TO 3.00 LPA
Production Executive
Company: Concept Pharma Pvt. Ltd. Location: Aurangabad Vacancy: 1 Experience: 2–3 Years CTC (Budget): ₹Negotiable
Key Responsibilities
Oversee day-to-day production activities to ensure adherence to production plans, batch records, and schedules.
Manage packaging operations to achieve quality standards and production targets while strictly following GMP norms.
Coordinate with the Production Planning and Quality ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
5.00 LPA TO 7.00 LPA
Job Description – R&D Parenteral (Formulation) Specialist
Company: Concept Pharma Pvt. Ltd. Position: R&D Parenteral (Formulation) Specialist Experience: 2–5 Years CTC (Budget): Negotiable Location: Aurangabad
Key Responsibilities
Support the R&D team in formulation development of parenteral products, including Small Volume Parenterals (SVP) and Large Volume Parenterals (LVP) in both powder and liquid dosage forms.
Perform sterile ...
1 Opening(s)
7.0 Year(s) To 12.0 Year(s)
Not Disclosed by Recruiter
The job description is as below:
The R&D Manager - NDDS will lead formulation and development of novel drug delivery systems, from concept to scale up and tech transfer, ensuring compliance with regulatory and quality standards and alignment with business goals. The role requires strong scientific depth in NDDS, team leadership ...
1 Opening(s)
3.0 Year(s) To 4.0 Year(s)
Not Disclosed by Recruiter
JD: Fitter, Plant Maintenance, Breakdown, Fitting
Company Profile:MNC pharmaceutical industry, the discovery, development, and manufacture of drugs and medications
Other Details :Work Timing – 8 hours (3 shifts)Working Days – 6 Days (1 rotational off)Location – Ahmedabad, SanandPayroll company- Talisman HR Solutions PVT LTD (Third Party Payroll)
Kindly provide your confirmation on the same.
4 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 4.00 LPA
Perform routine analysis of raw materials, in-process, and finished products
Operate and handle analytical instruments such as HPLC, GC, Karl Fischer, UV, Particle Size Analyzer, etc.
Ensure testing as per approved specifications, SOPs, and pharmacopeial requirements
Maintain proper documentation, test records, and compliance with GMP/GLP
Basic understanding of pharmaceutical formulations and related quality requirements
Support ...
4 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 4.00 LPA
Perform routine analysis of raw materials, in-process, and finished products
Operate and handle analytical instruments such as HPLC, GC, Karl Fischer, UV, Particle Size Analyzer, etc.
Ensure testing as per approved specifications, SOPs, and pharmacopeial requirements
Maintain proper documentation, test records, and compliance with GMP/GLP
Basic understanding of pharmaceutical formulations and related quality requirements
Support ...