Senior Officer Bosch Pharmaceuticals Karachi

Website Bosch Pharmaceuticals

Are you an experienced Quality Control (QC) professional with a background in Analytical Chemistry or Pharmacy? Are you looking to work with a reputable pharmaceutical company where quality, compliance, and innovation are at the heart of every product? Bosch Pharmaceuticals is inviting applications for the position of Senior Officer / Executive Quality Control for its Karachi-based manufacturing facility.

This opportunity is ideal for professionals who have 2–4 years of experience in pharmaceutical quality control laboratories and possess expertise in analytical testing, pharmaceutical regulations, Good Laboratory Practices (GLP), ISO standards, laboratory documentation, and analytical instrumentation.

If you are passionate about ensuring the safety, efficacy, and quality of pharmaceutical products while advancing your career in one of Pakistan’s growing pharmaceutical organizations, this role could be the perfect next step.


About Bosch Pharmaceuticals

Bosch Pharmaceuticals is a well-established pharmaceutical company committed to manufacturing high-quality medicines that meet both national and international quality standards. The company focuses on innovation, research, quality assurance, and regulatory compliance to deliver safe and effective healthcare products.

Bosch operates modern manufacturing facilities equipped with advanced laboratory instruments and follows internationally recognized pharmaceutical quality systems. Employees benefit from a professional working environment, opportunities for continuous learning, and exposure to modern analytical technologies.

Working in the Quality Control department means contributing directly to patient safety by ensuring that every product released to the market meets stringent quality specifications.


Job Overview

The Senior Officer / Executive Quality Control will perform laboratory analysis of raw materials, in-process samples, finished pharmaceutical products, and stability samples. The selected candidate will also prepare analytical reports, maintain laboratory documentation, operate sophisticated analytical equipment, and ensure compliance with Good Laboratory Practices (GLP), ISO standards, and pharmaceutical regulatory requirements.

This role requires strong analytical skills, technical expertise, attention to detail, and the ability to troubleshoot laboratory instruments while maintaining high standards of quality and compliance.


Job Title

Senior Officer / Executive Quality Control


Company

Bosch Pharmaceuticals


Job Location

Karachi, Pakistan

This is a full-time, on-site position.


Employment Type

  • Full-Time
  • Permanent Position

Educational Qualifications

Applicants should possess one of the following qualifications:

  • Bachelor of Science (B.Sc.) in Analytical Chemistry
  • Master of Science (M.Sc.) in Analytical Chemistry
  • Doctor of Pharmacy (PharmD)

Candidates with additional certifications in Quality Control, Analytical Instrumentation, ISO Quality Management Systems, or Good Laboratory Practices will have an added advantage.


Experience Required

Candidates should have:

  • 2–4 years of relevant pharmaceutical Quality Control experience
  • Experience working in pharmaceutical QC laboratories
  • Knowledge of analytical testing procedures
  • Experience with laboratory documentation
  • Familiarity with pharmaceutical regulations

Professionals currently working in pharmaceutical manufacturing companies will be preferred.


Required Technical Skills

The ideal candidate should possess expertise in:

  • Pharmaceutical Quality Control
  • Analytical Chemistry
  • Finished Product Testing
  • Raw Material Analysis
  • In-Process Quality Testing
  • Stability Studies
  • Laboratory Documentation
  • Standard Operating Procedures (SOPs)
  • Good Laboratory Practices (GLP)
  • ISO Standards
  • Data Recording and Reporting
  • Analytical Method Execution
  • Instrument Calibration
  • Laboratory Safety
  • Regulatory Compliance
  • Root Cause Analysis
  • Quality Investigation

Experience with computerized laboratory systems and electronic documentation is an additional advantage.


Knowledge of Analytical Instruments

The selected candidate should have practical experience operating and troubleshooting pharmaceutical laboratory equipment such as:

  • High Performance Liquid Chromatography (HPLC)
  • Gas Chromatography (GC)
  • UV-Visible Spectrophotometer
  • Fourier Transform Infrared Spectroscopy (FTIR)
  • Dissolution Test Apparatus
  • pH Meter
  • Karl Fischer Titrator
  • Analytical Balance
  • Moisture Analyzer

Hands-on knowledge of instrument qualification, calibration, and routine maintenance will be highly valuable.


Essential Soft Skills

Successful candidates should demonstrate:

  • Excellent analytical thinking
  • Strong attention to detail
  • Problem-solving abilities
  • Technical report writing skills
  • Effective communication
  • Teamwork and collaboration
  • Time management
  • Organizational skills
  • Decision-making capability
  • Ability to work under pressure
  • Commitment to quality and compliance

Key Responsibilities

The Senior Officer / Executive Quality Control will play a critical role in ensuring that pharmaceutical products meet all quality and regulatory requirements before being released to the market.


1. Finished Product Analysis

The selected candidate will:

  • Perform laboratory testing of finished pharmaceutical products.
  • Verify product quality against approved specifications.
  • Ensure products meet regulatory requirements.
  • Report any deviations or non-conformities.

Finished product analysis is essential for ensuring patient safety and product effectiveness.


2. Raw Material Testing

Responsibilities include:

  • Testing incoming raw materials.
  • Verifying material identity and purity.
  • Confirming compliance with approved specifications.
  • Supporting procurement and production through timely analysis.

Only approved raw materials should be released for manufacturing.


3. In-Process Quality Control

The Quality Control Officer will:

  • Analyze samples collected during production.
  • Monitor manufacturing quality.
  • Detect deviations early.
  • Support production teams in maintaining consistent product quality.

In-process testing minimizes production losses and ensures process consistency.


4. Stability Sample Testing

The selected candidate will conduct:

  • Long-term stability studies.
  • Accelerated stability testing.
  • Ongoing stability monitoring.
  • Shelf-life evaluation.

Stability studies ensure pharmaceutical products remain safe and effective throughout their intended storage period.


5. Laboratory Documentation

The role includes preparing and maintaining:

  • Analytical reports.
  • Laboratory notebooks.
  • Test records.
  • Certificates of Analysis (COA).
  • Equipment logbooks.
  • Investigation reports.
  • Quality documentation.

Proper documentation is essential for regulatory compliance and successful inspections.


6. SOP Preparation and Review

Responsibilities include:

  • Drafting Standard Operating Procedures (SOPs).
  • Updating existing SOPs.
  • Reviewing laboratory procedures.
  • Ensuring compliance with approved methods.
  • Supporting continuous improvement initiatives.

Well-written SOPs promote consistency and laboratory excellence.


7. Compliance with GLP

The candidate will ensure full compliance with Good Laboratory Practices (GLP) by:

  • Following approved laboratory procedures.
  • Maintaining accurate documentation.
  • Ensuring traceability of test results.
  • Following proper sample handling procedures.
  • Maintaining laboratory cleanliness and organization.

GLP compliance ensures reliable and reproducible laboratory results.


8. Compliance with ISO Standards

The selected candidate will support compliance with relevant ISO quality management standards by:

  • Following quality procedures.
  • Supporting internal audits.
  • Maintaining quality records.
  • Participating in corrective and preventive action programs.

ISO compliance strengthens laboratory quality systems and customer confidence.


9. Analytical Instrument Operation

The role requires operation of sophisticated laboratory instruments while ensuring:

  • Proper calibration.
  • Accurate analysis.
  • Routine maintenance.
  • Instrument performance verification.
  • Safe operation.

Efficient instrument utilization contributes to accurate laboratory results.


10. Instrument Troubleshooting

The Quality Control Officer will:

  • Identify equipment issues.
  • Perform basic troubleshooting.
  • Coordinate repairs with maintenance teams.
  • Document instrument problems.
  • Minimize laboratory downtime.

Strong troubleshooting skills improve laboratory efficiency and productivity.


11. Regulatory Compliance

The selected candidate will ensure laboratory activities comply with:

  • Pharmaceutical regulations.
  • Company quality policies.
  • National regulatory guidelines.
  • Good Manufacturing Practices (GMP).
  • Good Laboratory Practices (GLP).
  • ISO standards.

Regulatory compliance is essential for successful inspections and product approvals.


12. Continuous Quality Improvement

The candidate will actively participate in:

  • Process improvement initiatives.
  • Laboratory efficiency projects.
  • Root cause investigations.
  • Corrective and Preventive Actions (CAPA).
  • Quality risk management activities.

Continuous improvement helps enhance laboratory performance and maintain high-quality standards.


Why Join Bosch Pharmaceuticals?

Joining Bosch Pharmaceuticals offers several career benefits:

  • Work with a respected pharmaceutical manufacturer.
  • Gain experience with advanced analytical technologies.
  • Build expertise in pharmaceutical quality systems.
  • Strengthen knowledge of GLP, GMP, and ISO standards.
  • Work in a professional laboratory environment.
  • Develop your technical and leadership skills.
  • Contribute directly to patient safety and product quality.
  • Access long-term career growth opportunities within the pharmaceutical industry.

Who Should Apply?

This opportunity is ideal for professionals currently working as:

  • Quality Control Officer
  • Senior QC Officer
  • QC Executive
  • Laboratory Analyst
  • Analytical Chemist
  • Quality Assurance Officer
  • Pharmaceutical Analyst
  • QC Chemist
  • Stability Analyst
  • Microbiology & QC Professional (with analytical testing experience)

Candidates from pharmaceutical manufacturing, healthcare, biotechnology, chemicals, nutraceuticals, and laboratory testing organizations are encouraged to apply.


Tips for a Successful Application

Before submitting your application, make sure your resume highlights:

  • Experience with pharmaceutical quality control.
  • Hands-on operation of analytical instruments such as HPLC, GC, FTIR, or UV spectrophotometers.
  • Knowledge of GLP, GMP, and ISO standards.
  • Experience in raw material, in-process, finished product, and stability testing.
  • SOP preparation and documentation experience.
  • Regulatory inspection or audit participation.
  • Laboratory investigation and problem-solving achievements.
  • Analytical method execution and reporting skills.

Where possible, include measurable achievements such as improving laboratory efficiency, reducing testing turnaround time, supporting successful regulatory audits, or implementing process improvements.


How to Apply

Interested candidates should submit their updated resume by scanning the official QR code provided in the job advertisement.

Before applying, ensure your CV is updated with your educational qualifications, laboratory experience, analytical instrument expertise, regulatory knowledge, and key professional achievements.

As no closing date has been mentioned, candidates are encouraged to apply as early as possible.


Final Thoughts

The Senior Officer / Executive Quality Control position at Bosch Pharmaceuticals offers an excellent opportunity for professionals seeking to build a successful career in pharmaceutical quality control and analytical laboratory operations. With responsibilities covering finished product testing, raw material analysis, stability studies, SOP preparation, GLP compliance, ISO standards, analytical instrument handling, and regulatory documentation, this role provides valuable exposure to modern pharmaceutical manufacturing practices.

If you have 2–4 years of relevant experience, a qualification in Analytical Chemistry or PharmD, and a commitment to delivering high-quality pharmaceutical products, this could be the ideal opportunity to advance your career. Prepare a comprehensive, achievement-focused resume and apply promptly to become part of Bosch Pharmaceuticals’ quality-driven team.

To apply for this job please visit bosch-pharma.com.

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