Oxalis Hiring QC & Production

Oxalis Labs Hiring QC & Production | B.Pharm ITI | Baddi

Oxalis Labs hiring Quality Control Officers and Production Operators in Baddi. B.Pharm, M.Sc, ITI candidates with 2–5 years experience can apply.

Pharmaceutical professionals looking for career opportunities in Quality Control and Production can explore the latest openings announced by Oxalis Labs, a reputed pharmaceutical manufacturing company based in Baddi, Himachal Pradesh. The company is currently hiring experienced candidates for Quality Control Officer/Senior Officer and Production Operator positions at its USFDA and EU-GMP approved manufacturing facility.

This recruitment drive is ideal for candidates with experience in pharmaceutical quality control, finished goods testing, stability studies, granulation operations, and regulated manufacturing environments. Professionals seeking pharma jobs in Baddi, quality control analyst jobs, production operator vacancies, GMP manufacturing careers, and pharmaceutical manufacturing opportunities can apply for these positions.

Company Overview

Oxalis Labs is a well-established pharmaceutical manufacturing company known for producing high-quality healthcare products while maintaining international regulatory standards. The company operates manufacturing facilities that comply with stringent USFDA and EU-GMP requirements, ensuring quality, safety, and regulatory compliance across all production processes.

Working with Oxalis Labs provides exposure to regulated pharmaceutical manufacturing operations, quality management systems, documentation practices, and modern production technologies. Employees benefit from a professional work environment focused on quality excellence, operational efficiency, and career development.

For professionals aiming to build a long-term career in pharmaceutical manufacturing, quality assurance, quality control, and GMP operations, Oxalis Labs offers valuable industry experience and growth opportunities.

Job Role & Responsibilities

Quality Control Officer / Senior Officer

Qualification: B.Pharm or M.Sc

Experience: 2 to 5 Years

Key Responsibilities

• Perform testing of Finished Goods (FG) as per approved specifications.
• Conduct stability sample analysis and documentation.
• Ensure compliance with GMP, GLP, and regulatory requirements.
• Review analytical data and maintain laboratory records.
• Participate in investigation of deviations and out-of-specification results.
• Support audit readiness and quality compliance activities.
• Handle laboratory instruments and maintain analytical documentation.
• Follow SOPs and quality management system requirements.

Production Operator

Qualification: 12th Pass / ITI

Experience: 2 to 5 Years

Key Responsibilities

• Perform granulation activities as per batch manufacturing records.
• Operate and monitor production equipment.
• Ensure compliance with GMP and safety procedures.
• Maintain production logbooks and batch documentation.
• Monitor process parameters during manufacturing.
• Support production targets while maintaining product quality.
• Follow cleaning, line clearance, and documentation procedures.
• Coordinate with QA, QC, and engineering teams when required.

Eligibility / Qualifications

Educational Qualification

Quality Control

• B.Pharm
• M.Sc

Production

• ITI
• 12th Pass

Relevant Courses

B.Pharm, M.Pharm, Pharmaceutical Analysis, Pharmaceutical Chemistry, Analytical Chemistry, Industrial Chemistry, M.Sc Chemistry, Quality Assurance, Quality Control, GMP Compliance, Pharmaceutical Manufacturing, Industrial Pharmacy, ITI Mechanical, ITI Electrical, Production Technology.

Experience Requirements

• Quality Control Officer/Senior Officer: 2 to 5 Years
• Production Operator: 2 to 5 Years

Required Skills

Quality Control

• Finished Goods (FG) Testing
• Stability Analysis
• GMP Documentation
• Quality Compliance
• Regulatory Environment Knowledge

Production

• Granulation Operations
• Production Equipment Handling
• Batch Documentation
• GMP Compliance
• Manufacturing Process Monitoring

Preferred Candidate Profile

• Experience in USFDA-approved pharmaceutical facilities.
• Exposure to EU-GMP manufacturing environments.
• Strong understanding of pharmaceutical documentation practices.
• Good communication and teamwork skills.
• Ability to work in regulated manufacturing environments.

Why Join Oxalis Labs?

Oxalis Labs offers professionals an opportunity to work in a globally compliant pharmaceutical manufacturing environment. Employees gain valuable exposure to international quality standards, regulatory compliance requirements, and modern pharmaceutical manufacturing practices.

Key Benefits

• Work in a USFDA and EU-GMP approved facility.
• Exposure to international pharmaceutical standards.
• Stable career growth opportunities.
• Professional pharmaceutical manufacturing environment.
• Experience with regulated quality systems.
• Learning opportunities in GMP-compliant operations.
• Competitive compensation based on experience.

Location & Salary

Location: Baddi, Himachal Pradesh

Salary: Approx. ₹2.5 LPA – ₹6.5 LPA (Based on qualification, experience, and interview performance)

Application Process

Interested candidates can apply by sharing their updated resume along with current CTC details.

Apply Via Email

Email: devender.kumar@oxalislabs.co.in

Apply Via WhatsApp

WhatsApp: 8219249371

Important Instructions

• Mention your current CTC while applying.
• Ensure your resume highlights relevant pharmaceutical experience.
• Candidates with USFDA and EU-GMP exposure will be preferred.
• Apply as early as possible as positions are being filled on an urgent basis.

Frequently Asked Questions (FAQs)

1. Which positions are currently open at Oxalis Labs?

The company is hiring Quality Control Officer/Senior Officer and Production Operator professionals.

2. What qualification is required for the Quality Control role?

Candidates must possess a B.Pharm or M.Sc qualification with 2–5 years of relevant experience.

3. What qualification is required for the Production Operator role?

Candidates with ITI or 12th Pass qualifications and 2–5 years of production experience can apply.

4. Is regulatory manufacturing experience preferred?

Yes. Experience in USFDA and EU-GMP approved pharmaceutical manufacturing facilities is preferred.

5. What is the work location?

The positions are based at Oxalis Labs, Baddi, Himachal Pradesh.

6. How can I apply?

Candidates can send their CV to devender.kumar@oxalislabs.co.in or WhatsApp their details to 8219249371 along with their current CTC.

Category	Details
Company	Oxalis Labs
Department Vacancies	Quality Control Officer/Senior Officer, Production Operator
Qualification	B.Pharm, M.Sc, ITI, 12th Pass
Experience	2–5 Years
Location	Baddi, Himachal Pradesh