Oxalis Hiring QC Stability & FG

Oxalis Labs has announced a new hiring opportunity for experienced pharmaceutical professionals in the Quality Control department at its USFDA-approved manufacturing facility located in Baddi, Himachal Pradesh. The company is currently recruiting candidates for Stability and Finished Goods (FG) sections for Officer and Senior Officer positions.

This pharmaceutical hiring update is highly relevant for candidates searching for Quality Control jobs in pharma, QC Stability jobs, Finished Goods analysis jobs, USFDA plant jobs, B.Pharm jobs in Baddi, M.Sc pharma jobs, and pharmaceutical analytical laboratory careers in India.

Candidates with experience in regulated pharmaceutical manufacturing facilities and strong exposure to analytical testing, stability studies, finished product analysis, and GMP-compliant laboratory operations are encouraged to apply.

The hiring drive is aimed at professionals who want to build long-term careers in pharmaceutical quality systems, analytical testing, stability analysis, regulatory compliance, and pharmaceutical manufacturing support.

Applicants with B.Pharm, M.Pharm, or M.Sc qualifications and 1 to 7 years of pharmaceutical industry experience are eligible for these positions.

Company Overview

Oxalis Labs is a pharmaceutical manufacturing company known for operating a USFDA-approved production facility with a strong focus on quality, compliance, and regulated pharmaceutical manufacturing.

The company manufactures pharmaceutical formulations while maintaining strict adherence to:

• USFDA regulatory guidelines
• Good Manufacturing Practices (GMP)
• Pharmaceutical quality systems
• Analytical laboratory compliance
• Data integrity standards
• Stability monitoring systems

Pharmaceutical companies operating under regulated market approvals require highly efficient Quality Control teams to maintain analytical accuracy, documentation compliance, and product quality standards.

Oxalis Labs focuses on maintaining consistent quality standards across its pharmaceutical manufacturing and testing operations.

Working in a USFDA-approved pharmaceutical facility gives professionals practical exposure to:

• Regulatory audit preparedness
• Analytical laboratory systems
• Stability testing protocols
• Pharmaceutical compliance documentation
• GMP-controlled operations
• Finished product quality testing

Professionals looking to strengthen their experience in pharmaceutical analytical quality control and regulated manufacturing environments may find this opportunity valuable for long-term career growth.

Job Role & Responsibilities

Oxalis Labs is hiring for Quality Control roles in the Stability and Finished Goods sections.

Selected candidates will work as Officer or Senior Officer depending on their experience, technical knowledge, and pharmaceutical laboratory exposure.

Key Responsibilities

Candidates selected for these pharmaceutical QC positions will be responsible for:

• Performing stability sample analysis
• Conducting finished goods testing
• Supporting analytical laboratory activities
• Maintaining laboratory documentation
• Following GMP and GLP procedures
• Handling analytical instruments
• Supporting regulatory compliance activities
• Monitoring analytical test records
• Assisting in audit preparation
• Reviewing laboratory reports and test results

Stability Section Responsibilities

Professionals working in the Stability section may handle:

• Stability sample withdrawals
• Stability protocol execution
• Long-term and accelerated stability studies
• Stability chamber monitoring
• Trend analysis and reporting
• Documentation maintenance
• Product quality evaluation during stability studies

Finished Goods (FG) Testing Responsibilities

Candidates working in the FG section may perform:

• Finished product analysis
• Analytical testing procedures
• Dissolution testing
• Assay analysis
• Instrument calibration support
• Sample management activities
• Batch release testing support

Regulatory & GMP Exposure

The company is looking for candidates with knowledge of:

• GMP documentation
• Pharmaceutical quality systems
• Regulatory laboratory compliance
• Data integrity practices
• Laboratory investigation systems
• Pharmaceutical analytical standards

Candidates with exposure to regulated pharmaceutical manufacturing plants may receive preference during the selection process.

Eligibility / Qualifications

Candidates interested in applying for Oxalis Labs QC jobs should meet the following eligibility requirements.

Educational Qualification

• B.Pharm
• M.Pharm
• M.Sc

Relevant Courses

Pharmaceutical Analysis, Pharmaceutical Chemistry, Analytical Chemistry, Pharmaceutics, Industrial Pharmacy, Quality Assurance, Quality Control, Regulatory Affairs, Pharmaceutical Quality Systems, Instrumental Analysis, Pharmaceutical Manufacturing

Experience Required

• 1 to 7 years of pharmaceutical industry experience
• Experience in Quality Control departments is preferred
• Experience in Stability or Finished Goods sections may receive preference

Preferred Skills

Candidates with the following skills are preferred:

• Stability testing knowledge
• Finished product analysis
• GMP documentation
• Analytical laboratory handling
• Regulatory compliance awareness
• Pharmaceutical quality systems
• Data review and reporting
• Instrument handling knowledge
• Laboratory documentation practices

Why Candidates Should Apply

The pharmaceutical Quality Control sector remains one of the most critical areas in regulated pharmaceutical manufacturing.

Companies operating USFDA-approved manufacturing plants require experienced QC professionals capable of maintaining analytical accuracy and ensuring compliance with global pharmaceutical standards.

Professionals joining Oxalis Labs may gain exposure to:

• USFDA-regulated manufacturing systems
• Pharmaceutical analytical laboratories
• Stability testing operations
• GMP-controlled work environments
• Regulatory quality systems
• Advanced pharmaceutical testing procedures
• Audit compliance activities

Quality Control professionals with regulated market exposure often receive strong career growth opportunities in:

• Pharmaceutical analytical development
• Quality assurance systems
• Regulatory compliance management
• Stability management programs
• Laboratory operations leadership

Work Environment & Career Growth

Oxalis Labs offers a regulated pharmaceutical work environment focused on analytical precision, quality systems, and compliance-driven operations.

Professionals working in QC laboratories gain hands-on exposure to:

• Analytical documentation systems
• Pharmaceutical regulatory standards
• Stability management programs
• Laboratory compliance procedures
• Product quality evaluation
• Pharmaceutical testing systems
• Audit preparation activities

Candidates demonstrating strong analytical knowledge and compliance awareness may receive opportunities for career advancement in pharmaceutical quality management and laboratory leadership roles.

Location & Salary

Job Location

Baddi, Himachal Pradesh

Salary

Salary will be offered according to candidate experience, analytical expertise, regulatory exposure, and current pharmaceutical industry standards.

Application Process

Interested and eligible candidates can apply through WhatsApp or email.

Contact Number

8219249371

Email ID

devender.kumar@oxalislabs.co.in

Documents Recommended While Applying

Candidates should share:

• Updated resume
• Educational qualification documents
• Experience certificates
• Current salary details
• Contact information

Important Note

Candidates with prior exposure to pharmaceutical Quality Control laboratories, Stability testing, or Finished Goods analysis may receive preference during the recruitment process.

FAQs

1. Which department is hiring at Oxalis Labs?

Oxalis Labs is hiring for the Quality Control department.

2. Which sections are available in QC?

The company is hiring for Stability and Finished Goods (FG) sections.

3. What qualifications are required?

Candidates with B.Pharm, M.Pharm, or M.Sc qualifications are eligible.

4. What experience is required for these pharma jobs?

Candidates should have 1 to 7 years of pharmaceutical industry experience.

5. Is this a USFDA-approved pharmaceutical facility?

Yes. Oxalis Labs operates a USFDA-approved manufacturing facility.

6. How can candidates apply?

Candidates can apply through WhatsApp or email by sharing their updated resume.

Summary Table

Company	Oxalis Labs
Department Vacancies	Quality Control – Stability / FG
Qualification	B.Pharm, M.Pharm, M.Sc
Experience	1 to 7 Years
Location	Baddi