Thinq Pharma Hiring QC, QA (Documentation, QAMS, IPQA), Microbiology Analyst, Microbiology QA

API Pharma Jobs for BSc, MSc, B Pharm Candidates | Thinq Pharma Pithampur Vacancies

Explore current API pharma job openin    gs at Thinq Pharma’s USFDA-approved plant in Pithampur for BSc, MSc, B Pharm graduates. Apply now with 1–7 years of experience.

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Explore Career Opportunities at Thinq Pharma’s USFDA-Approved API Manufacturing Facility

Thinq Pharma is actively hiring qualified professionals for various roles in its API manufacturing plant located in Pithampur. With a strong presence in the pharmaceutical industry and a USFDA-approved facility, the company offers a great platform for professionals with backgrounds in BSc, MSc (Microbiology/Biotech), or B Pharm to grow and contribute to quality-driven operations.

These job opportunities span across Quality Control (QC), Quality Assurance (QA), Microbiology, and Documentation roles, making it ideal for candidates with 1–7 years of relevant API industry experience. Thinq Pharma also welcomes freshers in microbiology and biotech for analyst positions.

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Current Vacancies at Thinq Pharma – API Division

Quality Control (QC) Analyst – HPLC & GC

• Experience Required: 4–5 years
• Responsibilities:
  • Perform routine analysis using HPLC and GC techniques.
  • Ensure compliance with cGMP and regulatory standards.
  • Prepare and review analytical reports.

Quality Assurance (QA) – QAMS & Documentation

• Experience Required: 4–6 years
• Responsibilities:
  • Manage quality assurance documentation.
  • Support compliance for regulatory audits.
  • Handle deviations, CAPA, and change controls.

IPQA Executive

• Experience Required: 3–4 years
• Responsibilities:
  • In-process checks during manufacturing and packaging.
  • Documentation review for batch records.

QA Documentation Officer

• Experience Required: 1 year
• Responsibilities:
  • Maintain QA documentation system.
  • Assist in audit readiness and regulatory filings.

QA – Operations Documentation

• Experience Required: 5–7 years
• Responsibilities:
  • Maintain and control all operational documentation.
  • Ensure GMP compliance across operational SOPs.

Microbiology Lab QA

• Experience Required: 2–3 years
• Educational Qualification: MSc in Microbiology or Biotech
• Responsibilities:
  • Handle microbiological documentation and validations.
  • Support lab investigations and audits.

Microbiology Analyst – Freshers

• Educational Qualification: MSc in Microbiology or Biotech
• Experience: Freshers welcome
• Responsibilities:
  • Conduct routine microbiological testing.
  • Prepare reports under supervision.

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Key Requirements

Required Educational Qualifications:

• BSc / MSc in Microbiology, Biotechnology, or related life sciences
• B Pharm with relevant analytical or QA background

Experience:

• Minimum 1 year to 7 years of API industry experience depending on the role
• Freshers eligible for Analyst role in Microbiology

Location:

• Pithampur, Madhya Pradesh

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Why Join Thinq Pharma?

• Work in a USFDA-approved environment
• Be part of a company with strong compliance and documentation culture
• Contribute to global quality standards
• Opportunity for career growth in QA/QC/Microbiology

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How to Apply

Interested candidates can email their updated resumes to: bhakti.patki@thinqcro.com

Please mention your role of interest in the subject line for faster processing.

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Summary Table

Company Name	Thinq Pharma
Current Vacancies	QC, QA (Documentation, QAMS, IPQA), Microbiology Analyst, Microbiology QA
Required Education	BSc, MSc (Microbiology/Biotech), B Pharm
Experience Required	0–7 Years depending on role