Tiefenbacher Labs Hiring 50 QC Officers

M.Pharm/M.Sc QC Officer – Formulation | Hyderabad

Tiefenbacher Labs hiring 50 QC Officers (M.Pharm/M.Sc) for formulation analysis in Hyderabad. 3–5 yrs experience required.

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Tiefenbacher Laboratories is recruiting 50 Quality Control Officers/Executives (Formulation) for its analytical teams in Hyderabad. If you hold an M.Pharm or M.Sc and have 3–5 years of hands-on experience with HPLC, GC and other instrumental techniques, this is a high-impact role in a GMP-driven environment focused on formulation analysis and regulatory compliance.

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Company Overview

Tiefenbacher Laboratories is an established contract research and analytical services provider with strong capabilities in pharmaceutical testing and formulation analytics. The Hyderabad facility at Gaddapotharam, Kazipally Industrial Area supports both development and routine QC testing for oral and other dosage forms, serving pharma manufacturers, CROs, and regulatory submissions. The lab emphasizes Good Laboratory Practice (GLP), data integrity, and timely, defensible reporting — making it a trusted partner for quality-driven pharmaceutical operations.

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Job Role & Responsibilities

You will join the QC Formulation team and be responsible for routine and complex instrumental analysis that supports product quality, stability, and release decisions.

Position: Officer / Executive — Quality Control (Formulation)

Openings: 50
Experience: 3–5 years
Qualification: M.Pharm / M.Sc (Analytical, Pharmaceutics, Pharmaceutical Sciences, Chemistry)

Primary Responsibilities:

• Execute analytical testing for formulation batches using HPLC, GC, UV-Vis, FTIR and related instruments.
• Perform assay, related substances, dissolution, content uniformity and other formulation-specific tests.
• Maintain instrument suitability, calibration logs and preventive maintenance records.
• Prepare accurate analytical records, maintain LIMS entries and ensure data integrity.
• Investigate OOS (Out of Specification) / OOT (Out of Trend) results and support CAPA documentation.
• Follow GLP, SOPs and regulatory documentation practices for client-facing reports.
• Support stability studies and periodic reporting for long-term and accelerated conditions.
• Coordinate with QC leadership, QA and production teams for sample acceptance and release decisions.

Technical skills that matter: strong troubleshooting on HPLC/GC, method transfer experience, understanding of system suitability, and experience in instrument qualification or validation activities.

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Eligibility / Qualifications

Minimum Education: M.Pharm or M.Sc in Pharmaceutical Sciences, Pharmaceutics, Analytical Chemistry or equivalent.

Experience: 3–5 years of hands-on QC formulation analysis in a GLP / GMP environment.

Must-have competencies:

• Proficiency in HPLC, GC, UV, FTIR operation and routine maintenance.
• Sound knowledge of GLP, data integrity principles, and pharma documentation standards.
• Experience with OOS/OOT investigations and root-cause analysis.
• Good analytical reasoning, report-writing and familiarity with LIMS or ELN is preferred.

Nice-to-have: Exposure to stability protocol execution, basic knowledge of method validation, and prior work in a WHO/USFDA/MHRA-compliant facility.

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Location & Salary

Work Location: Tiefenbacher Laboratories, Survey No. 42, Gaddapotharam, Kazipally Industrial Area, Sanga Reddy District, Hyderabad – 502319, Telangana.
Salary: Competitive and aligned with industry standards; defined based on experience and technical fit.

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Application Process

Interested candidates should email an updated CV to k.surendra@tiefenbacher.com. Shortlisted candidates will be contacted for interview scheduling.

Contact:
Email: k.surendra@tiefenbacher.com
Phone: +91-8418694444

Documents to attach: Updated CV, copies of degree certificates, and experience proof (offer letters / payslips) where available.

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Why Join Tiefenbacher Laboratories?

• Large-volume hiring across QC gives scope for immediate onboarding and rapid team integration.
• Work with modern analytical instrumentation and well-defined GLP processes.
• Roles involve technical ownership — OOS investigations, method troubleshooting and stability analytics — which accelerates skill growth.
• Organization supports clear career paths into Senior QC, Method Development, or QA functions for high performers.
• Contribute directly to product quality and regulatory readiness — work that impacts patient safety and compliance.

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FAQs

Q1 — What is the minimum qualification required?
M.Pharm or M.Sc in relevant disciplines is required for this QC Formulation role.

Q2 — How many openings are there?
There are 50 openings for Officer / Executive level in Quality Control (Formulation).

Q3 — What experience is expected?
Candidates should have 3–5 years of hands-on experience with HPLC, GC, UV and FTIR in a GLP/GMP lab.

Q4 — Do I need experience with OOS/OOT investigations?
Yes. Practical exposure to OOS/OOT investigations and CAPA documentation is expected.

Q5 — How do I apply?
Email your CV to k.surendra@tiefenbacher.com. Include qualification, years of experience and current CTC in the email body.

Q6 — Will the company consider candidates from regulatory/contract labs?
Yes. Candidates from CROs, contract labs and pharma QC labs with relevant analytical experience are welcome.

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Summary Table

Category	Details
Company	Tiefenbacher Laboratories
Vacancies	Quality Control – Formulation (Officer / Executive) – 50 positions
Required Education	M.Pharm, M.Sc (Pharmaceutics, Pharmaceutical Analysis, Analytical Chemistry)
Experience	3–5 years (instrumental analysis: HPLC, GC, UV, FTIR)
Location	Gaddapotharam, Kazipally Industrial Area, Sanga Reddy District, Hyderabad
Email	k.surendra@tiefenbacher.com
Phone	+91-8418694444