Oxalis Hiring QA , Production

BPharm QA Production Jobs Oxalis Labs Baddi

B.Pharm/M.Pharm, ITI candidates apply for QA & Production roles at Oxalis Labs Baddi with 1–8 yrs experience.

Oxalis Labs is hiring for Quality Assurance (IPQA/Documentation) and Production (Granulation) roles at its USFDA-approved facility in Baddi, Himachal Pradesh. This is a strong opportunity for candidates seeking pharma jobs in Baddi, QA documentation roles, IPQA jobs, and OSD manufacturing careers in a regulated environment.

With the ongoing expansion of formulation manufacturing and increasing demand for GMP-compliant professionals, these openings provide hands-on exposure to pharmaceutical quality systems, batch manufacturing processes, and regulatory-driven production workflows.

Company Overview

Oxalis Labs is a pharmaceutical manufacturing company operating a USFDA-approved facility, known for its focus on quality, compliance, and global regulatory standards. The company manufactures oral solid dosage (OSD) formulations and follows strict GMP, WHO-GMP, and international regulatory guidelines.

Working at Oxalis Labs provides professionals with exposure to regulated markets, audit readiness practices, and advanced pharmaceutical manufacturing systems that directly impact patient safety and product quality.

Job Role & Responsibilities

Quality Assurance – IPQA / Documentation (Officer / Executive)

• Perform in-process quality assurance (IPQA) checks during manufacturing and packing operations
• Review batch manufacturing records (BMR) and batch packing records (BPR)
• Ensure compliance with GMP, SOPs, and regulatory guidelines
• Handle documentation control, deviation reports, and CAPA processes
• Support internal audits and regulatory inspections (USFDA / WHO-GMP)
• Monitor line clearance, in-process controls, and documentation accuracy

Production – Granulation (Operator)

• Execute granulation activities for OSD manufacturing (wet/dry granulation)
• Operate equipment such as RMG, FBD, blender, and milling machines
• Follow batch manufacturing instructions and SOPs
• Maintain cleanliness and safety standards in production areas
• Record process parameters and ensure consistency in batch processing
• Support troubleshooting and process optimization during manufacturing

Eligibility / Qualifications

Educational Qualification

• B.Pharm, M.Pharm (for QA roles)
• 12th / ITI (for Production Operator roles)
• Relevant Courses: Pharmaceutics, Pharmaceutical Quality Assurance, Industrial Pharmacy, GMP Compliance, Production Technology

Experience Required

• Quality Assurance: 1 to 8 years
• Production Operator: Minimum 1.7 years experience

Key Skills

• Strong knowledge of GMP, GLP, and regulatory compliance
• Experience in IPQA and documentation control systems
• Hands-on experience in OSD granulation processes
• Understanding of BMR/BPR, deviation handling, and CAPA
• Exposure to USFDA-approved plant operations (highly preferred)

Location & Salary

• Location: Baddi, Himachal Pradesh
• Salary: Competitive salary based on experience (₹2–10 LPA estimated)

Application Process

• Email your CV to: devender.kumar@oxalislabs.co.in
• WhatsApp: 8219249371
• Ensure your resume highlights GMP experience, IPQA exposure, and manufacturing skills

Why This Opportunity Stands Out

• Work in a USFDA-approved pharmaceutical manufacturing facility
• Strong exposure to IPQA, GMP compliance, and regulatory audits
• Growth opportunities in QA documentation and production operations
• Ideal for candidates aiming for careers in regulated pharma markets

Career Scope in QA & Production (SEO Boost Section)

Careers in pharmaceutical quality assurance and production are among the most stable and high-demand roles in the healthcare industry. Professionals with expertise in IPQA, GMP compliance, and OSD manufacturing are highly valued in USFDA, EU-GMP, and WHO-regulated facilities.

With increasing global demand for quality medicines, roles in QA documentation, validation, and production operations offer strong salary growth and long-term career security.

High CPC Keywords Naturally Included

• Pharmaceutical quality assurance jobs
• IPQA jobs in pharma industry
• GMP compliance roles
• OSD manufacturing jobs
• USFDA pharma jobs in India

FAQs

Who can apply for Oxalis Labs jobs?

Candidates with B.Pharm, M.Pharm, ITI, or 12th qualification with relevant experience can apply.

Is USFDA experience required?

Preferred, especially for QA roles, but not mandatory.

What is IPQA in pharma?

IPQA (In-Process Quality Assurance) ensures quality checks during manufacturing to maintain compliance.

What is the job location?

Baddi, Himachal Pradesh.

How to apply?

Candidates can apply via email or WhatsApp as provided.

Is QA role better than Production in pharma?

QA roles offer strong growth in compliance and regulatory careers, while production roles provide hands-on manufacturing expertise. Both have strong career paths depending on interest.

Additional SEO Titles

• QA IPQA Jobs in Baddi for BPharm MPharm Candidates
• Pharma Production Granulation Operator Jobs Himachal Pradesh
• USFDA Pharma Jobs in Baddi for Freshers and Experienced

Summary Table

Category	Details
Company	Oxalis Labs
Vacancies	QA Officer/Executive (IPQA/Documentation), Production Operator (Granulation)
Required Education	B.Pharm, M.Pharm, ITI, 12th
Experience	1–8 Years