What Jobs are available for Lucky Cement in Karachi?

Placement is one of a key HR function. Barrett Hodgson Pakistan thrives on its human resources for achieving its strategic and business objectives. It has a highly motivated team manning various departments who have clearly laid down roles to perform. The objective of a well-designed job is to enable management and staff to strive at their optimum to achieve desired results, we believe that;

• Our people are our most valuable asset.
• We view Human Resources as a competitive advantage.
• We ensure business goals are realized through people while meeting their own personal aspirations and development.
• We ensure only motivated and professionally qualified people are employed.
• Barrett Hodgson is an equal opportunity employer with policies to ensure there is no discrimination on the basis of caste, creed, sex, etc.

The objective is to hire the right person for the right job at the right time and place qualified and experienced individuals fulfilling the pre-determined standards demanded by the position and established by the Company. Selection process is transparent and done strictly on merit and No under age employment as per relevant laws is made/effective.

If you think you are meeting the job specification and requirements and have the passion for success and ability to perform and grow, apply now at

Quality Control (Microbiological Lab) – Executive / Sr. Officer

Candidate should be BS /M.Sc.(Microbiology) with 2-5 years experience in Micro Lab. and can work on microbiological instruments.

Qualification: B.Sc. (Hons.) or MSc. Food Science/ Microbiologists,

Experience: 1-2 years (Preferably in food sector)

Must Have Valid Motor Cycle License

A renowned FMCG is currently looking for a 'Quality Control Officer' for its warehouse in 'West Wharf Karachi' Incumbent should have done B.Sc./MSc. (Food Science) or Microbiologist. Ideal candidate should know different testing methods to check the quality and ensure that products meet food safety and nutritional standards.

Since this position is of warehouse so preference will be given to (Male) candidates only.

Job Type: Full-time

Work Location: In person

Job Purpose

To supervise the quality control activities of Lab Operations & ensure compliance as per cGMP, regulatory and QMS requirements for Site F-268.

Quality Control Incharge role is responsible for the requirements in accordance with the Local Regulations.

Education, Experience & Skills

• M.Sc. Chemistry or Pharm-D
• Minimum 10-years' experience of testing for M.Sc. Chemistry / Pharmacist of having 6 years' experience of testing.
• Computer literacy, minimum to access and utilize emails for official correspondence.
• Use of MS-Office (Word, Excel, PowerPoint) at least to a moderate level.
• Stakeholder management and good communication skills.
• Stay updated with the latest local regulatory standards and pharmacopoeia requirements and guidelines related to QC in the pharmaceutical industry.
• Ability to work in a fast-paced, highly regulated environment.
• Experience leading teams and managing laboratory operations

Key Responsibilities

• Oversight for the testing and release / rejection of incoming materials, intermediate, bulk, and finished products, and batch records for site and for contract manufacturing.
• Oversee the Quality control processes, including sampling, testing and inspection of raw material, finished Products & Utilities. Oversee specifications, test methods, and other quality control procedures. Ensure analysis is being carried out in compliance with the standards in case of any contract
• Perform & review of current standard related to QMS and local regulatory for Quality Control Lab.
• Perform and approve appropriate validations pertaining to Lab ops, including those of analytical procedures, cleaning method validation & Equipment validations. Ensure routine cleaning verification on time.
• Ensure timely completion of equipment calibrations and ensure DI Compliance
• Oversee the maintenance of the department, premises, and equipment.
• Oversight that the initial and continuing training of Quality personnel is carried out and adapted according to need Lead self-inspection process for the governance of Quality system in compliance with QMS and Local regulatory requirements.
• Responsible for the management and timely updation of legal agreements, quality agreements, and also responsible for third-party risk management.
• Ensure timely creation, submission, and approval of purchase orders to facilitate the availability of laboratory consumables and CAPEX items, ensuring uninterrupted laboratory operations.
• Provide support to ensure the timely preparation and submission of responses pertaining to laboratory operations for regulatory queries

Why GSK?

Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we're committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

Contact information:

You may apply for this position online by selecting the Apply now button.

Important notice to Employment businesses/ Agencies

GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

Senior Quality Control Officer/ Executive with an experience to 3 – 4years having hands on experience on HPLC trouble shootings and other analytical related issues and Method validation.

Job Type: Full-time

Work Location: In person

Placement is one of a key HR function. Barrett Hodgson Pakistan thrives on its human resources for achieving its strategic and business objectives. It has a highly motivated team manning various departments who have clearly laid down roles to perform. The objective of a well-designed job is to enable management and staff to strive at their optimum to achieve desired results, we believe that;

• Our people are our most valuable asset.
• We view Human Resources as a competitive advantage.
• We ensure business goals are realized through people while meeting their own personal aspirations and development.
• We ensure only motivated and professionally qualified people are employed.
• Barrett Hodgson is an equal opportunity employer with policies to ensure there is no discrimination on the basis of caste, creed, sex, etc.

The objective is to hire the right person for the right job at the right time and place qualified and experienced individuals fulfilling the pre-determined standards demanded by the position and established by the Company. Selection process is transparent and done strictly on merit and No under age employment as per relevant laws is made/effective.

If you think you are meeting the job specification and requirements and have the passion for success and ability to perform and grow, apply now at

Quality Control – Executive / Sr. Officer

Candidate should be Pharm-D / BS /M.Sc.(Chemistry) with 2-5 years experience in QC Lab and can work on HPLC, GC, FTIR, and other pharma related instruments

• Full responsibility for quality function within the location through the entire Sample process including finished Sample inspection, and testing.
• Maintains and improves product and operation quality by monitoring product requirements.
• Responsible for all Technical Audit and implementation of customer technical requirements.
• Should have knowledge of all aspects of quality control methods, practices and other prevailing international standards.

Job Type: Full-time

Work Location: In person