Acme Generics Hiring QC Officer/Executive

Pharma Stuff; Solan; On-site; INR 600,000 - 900,000; Full time

Job summary

Acme Generics is urgently hiring QC Officer/Executive for its Baddi facility. Candidates with B.Pharm or M.Sc and 2–5 years of QC experience in USFDA/EU‑GMP environments are preferred. The role covers finished product testing, AMV/AMT, stability studies, and data integrity within a regulated manufacturing setup.

Based in Baddi, Himachal Pradesh, the position offers exposure to global regulatory standards and a clear path for growth in analytical quality control.

Qualifications

• B.Pharm and M.Sc candidates with relevant QC exposure are eligible.
• 2–5 years of QC experience in USFDA and EU‑GMP regulated pharma plants.
• Experience in finished product testing and regulatory compliance is required.

Responsibilities

• Analyze finished products, raw materials and in‑process samples.
• Perform analytical method validation (AMV) and method transfer (AMT).
• Conduct stability studies per ICH and regulatory guidelines.
• Maintain GMP/compliant documentation and data integrity.

Skills

Finished Goods analysis

Analytical Method Validation

Analytical Method Transfer

Raw Material testing

Stability studies

Quality Management Systems

Education

B.Pharm

M.Sc

Job description

B.Pharm, M.Sc QC Officer Jobs in Baddi | Acme Generics
Acme Generics hiring QC Officer/Executive in Baddi. B.Pharm, M.Sc with 2–5 years experience. USFDA & EU‑GMP facility.

Acme Generics is urgently hiring experienced Quality Control professionals to strengthen its regulated manufacturing operations at its Baddi facility. This opportunity is ideal for candidates with hands‑on QC experience in USFDA and EU‑GMP approved pharmaceutical plants who are looking for stable, compliance-driven careers in analytical quality control. The role offers direct involvement in finished product testing, stability studies, and quality systems that support global pharmaceutical supply chains.

Company Overview

Acme Generics is a growing pharmaceutical manufacturing organization focused on delivering high‑quality generic medicines for regulated and semi‑regulated markets. The company operates with strong adherence to international regulatory standards, including USFDA and EU‑GMP guidelines, ensuring product quality, patient safety, and data integrity.

With a compliance‑oriented culture and emphasis on analytical excellence, Acme Generics provides professionals with exposure to regulated audits, robust quality systems, and long‑term career growth within pharmaceutical quality control operations.

Job Role & Responsibilities

Officer / Executive – Quality Control

The selected candidate will be responsible for routine and advanced quality control activities within a regulated manufacturing environment.

Key Responsibilities:

• Analysis of finished products, raw materials, and in‑process samples
• Execution of analytical method validation (AMV) and analytical method transfer (AMT)
• Stability studies as per ICH and regulatory guidelines
• Documentation and review of QC data in line with GMP and QMS requirements
• Compliance with USFDA and EU‑GMP regulations
• Support during internal, regulatory, and customer audits
• Maintenance of laboratory records, logbooks, and data integrity systems

This role plays a critical part in ensuring product quality and regulatory compliance for global pharmaceutical markets.

Eligibility / Qualifications

Required Education:

B.Pharm, M.Sc (Pharmaceutical Sciences or Chemistry related disciplines)

Experience Requirements:

• 2 to 5 years of relevant experience in pharmaceutical Quality Control
• Mandatory experience in USFDA and EU‑GMP approved manufacturing facilities

Key Skills:

• Finished Goods (FG) analysis
• Analytical Method Validation (AMV)
• Analytical Method Transfer (AMT)
• Raw Material (RM) testing
• Stability studies
• Quality Management Systems (QMS)

Location & Salary

• Job Location: Baddi, Himachal Pradesh
• Salary: Best in industry, based on experience, current CTC, and skill level

Exact compensation details will be discussed during the interview process.

FAQs

Who can apply for this QC role?
Candidates with 2–5 years of QC experience in USFDA and EU‑GMP regulated pharma plants can apply.

Is USFDA or EU‑GMP experience mandatory?
Yes. Experience in regulated manufacturing facilities is a mandatory requirement.

What qualifications are accepted?
B.Pharm and M.Sc candidates with relevant QC exposure are eligible.

Where is the job located?
The position is based at Acme Generics, Baddi.

Summary Table

• Company: Acme Generics
• Vacancies: Officer / Executive – Quality Control
• Required Education: B.Pharm, M.Sc
• Experience: 2–5 Years (USFDA