Oxalis walk-in Production,QC

ITI/B.Pharm QC Production Jobs Baddi Walk-in

ITI, Diploma, B.Pharm, M.Sc candidates apply for Production and QC jobs at Oxalis Labs Baddi. 2–6 yrs exp.

Oxalis Labs is conducting a plant walk-in drive for experienced professionals in Production OSD and Quality Control departments at its Baddi manufacturing facility. This is a strong opportunity for candidates searching for pharmaceutical production jobs, QC analyst careers, HPLC analyst jobs, and OSD manufacturing opportunities in a regulated pharmaceutical environment.

Candidates with experience in granulation, pharmaceutical manufacturing operations, and analytical testing using HPLC systems can build long-term careers in one of the growing pharmaceutical manufacturing hubs in India. The demand for professionals skilled in GMP production systems, analytical quality control, and pharmaceutical documentation continues to rise across the pharma industry.

Company Overview

Oxalis Labs is a pharmaceutical manufacturing company focused on quality-driven formulation and production operations. The company operates manufacturing facilities aligned with pharmaceutical quality systems and GMP compliance standards.

The Baddi pharmaceutical manufacturing hub is one of India’s major pharma production zones, offering professionals strong exposure to OSD manufacturing, quality assurance systems, analytical testing, and regulated production environments.

Working in pharmaceutical production and quality control functions helps professionals develop expertise in manufacturing operations, quality compliance, analytical instrumentation, and pharmaceutical regulatory systems.

Job Role & Responsibilities

Oxalis Labs is hiring for Production OSD and Quality Control departments.

Production OSD – Technical Associate / Operator

Key Responsibilities

• Handle granulation activities in OSD manufacturing
• Operate and monitor pharmaceutical production equipment
• Follow GMP guidelines and batch manufacturing procedures
• Maintain production documentation and process records
• Support compression and formulation manufacturing activities
• Ensure cleanliness, safety, and process compliance in manufacturing areas

Quality Control – QC Analyst / Officer / Sr. Officer

Key Responsibilities

• Perform analytical testing using HPLC systems
• Conduct analysis of raw materials, finished products, and in-process samples
• Ensure compliance with Good Laboratory Practices and cGMP standards
• Prepare and review analytical documentation and laboratory records
• Support investigations related to OOS, OOT, and analytical deviations
• Maintain calibration and laboratory compliance activities

These responsibilities directly contribute to pharmaceutical quality systems, product consistency, and regulatory-approved drug manufacturing.

Eligibility / Qualifications

Production OSD

• 10+2
• ITI
• Diploma
• Any Graduate

Quality Control

• B.Pharm
• M.Sc

Experience Requirement

• 2 to 6 years of relevant pharmaceutical manufacturing or QC experience

Relevant Courses

B.Pharm, M.Sc Chemistry, M.Sc Analytical Chemistry, Diploma in Mechanical Engineering, Diploma in Chemical Engineering, ITI Fitter, ITI Technician, B.Sc Chemistry

Required Skills

• GMP and pharmaceutical manufacturing knowledge
• Experience in granulation and OSD operations
• Hands-on expertise with HPLC analytical systems
• Knowledge of laboratory documentation and compliance
• Understanding of pharmaceutical quality systems and regulatory standards
• Good communication and teamwork skills

Location & Salary

Work Location: Oxalis Labs, Baddi, Himachal Pradesh

Salary: Competitive pharmaceutical production and QC salary package based on experience and technical expertise

Professionals with HPLC analytical experience and OSD manufacturing exposure are highly valued in regulated pharmaceutical manufacturing facilities.

Application Process

Walk-in Interview Details:

Date: 17 May 2026 (Sunday)
Time: 09:00 AM onwards

Venue:
OXALIS LABS
PO – Lodhimajra,
Himachal Pradesh – 174101

Documents Required

• Updated CV
• Salary structure (CTC breakup)
• Aadhaar card

Contact Details

• 8894725502
• 8219249371

Candidates are advised to attend early due to high competition for QC analyst and OSD manufacturing roles.

Why This Opportunity Matters

Pharmaceutical production and analytical quality control are among the most stable and high-demand domains in the pharma industry. Professionals with expertise in HPLC testing, granulation operations, and GMP manufacturing systems are highly sought after by pharmaceutical companies.

Working in OSD manufacturing and QC laboratories strengthens expertise in pharmaceutical compliance management, analytical science, and production quality systems. These skills significantly improve long-term career opportunities in multinational pharmaceutical companies and regulated manufacturing environments.

Quality Control roles involving analytical instrumentation and HPLC operations are especially valuable because of their direct impact on product quality, regulatory approvals, and patient safety.

Key Highlights

• Company: Oxalis Labs
• Departments: Production OSD, Quality Control
• Roles: Technical Associate, Operator, QC Analyst, Officer, Sr. Officer
• Qualification: ITI, Diploma, B.Pharm, M.Sc
• Experience: 2–6 Years
• Industry: Pharmaceutical Manufacturing
• Location: Baddi, Himachal Pradesh
• Walk-in Date: 17 May 2026

FAQs

Who can apply for Oxalis Labs jobs?

Candidates with ITI, Diploma, B.Pharm, M.Sc, or graduation qualifications and relevant pharma experience can apply.

What experience is required?

2 to 6 years of experience in pharmaceutical production or QC analytical testing.

What technical skills are preferred?

Granulation, HPLC handling, GMP documentation, analytical testing, and OSD manufacturing operations.

Are HPLC skills mandatory for QC roles?

Yes, hands-on experience in HPLC analytical testing is required.

How can I apply?

Candidates can directly attend the walk-in interview with the required documents.

Summary Table

|———————————-|———————————-|
| Company | Oxalis Labs |
| Vacancies | Technical Associate, Operator, QC Analyst, Officer, Sr. Officer |
| Required Education | ITI, Diploma, B.Pharm, M.Sc |

Experience	2–6 Years