77 Laboratory Analyst jobs in Pakistan

Siddiq Leather Works (Pvt) Ltd., Pakistan

Key activities related to the wet-end department include improvements in chemical processing, problem-solving, and cost control methods in formulations. A strong concept of chemistry involved in leather technology is essential to understand and resolve issues.

Must be a Graduate/Master Degree Holder from a leading university.

Position will be responsible for new product development and will work closely with merchandisers, production, and other cross-functional departments. The individual will lead Research & Development after the R&D manager.
Position will report to the R&D Manager.

Must have a bachelor’s/master’s degree with at least 3-4 years of relevant experience, preferably in the knitted & woven garments/sportwear industry. Must have good knowledge of MS Office.

Khurrianwala, Pakistan | Posted on 11/26/2024

Nutrifactor has been manufacturing nutraceutical products, vitamins, minerals and other natural health care products for more than 10 years. Our 30+ years of expertise in family owned pharmaceutical business has enabled us to identify industry trends far ahead of the competition. Nutrifactor has invested heavily in extensive manufacturing, well equipped laboratory, modern instruments, efficient distribution and warehousing capabilities that position us for future growth and allow us to serve better both domestically and internationally.

We are seeking a dynamic and skilled Assistant Manager Research & Development (R&D) to support the development and optimization of pharmaceutical products. This role involves assisting in managing formulation projects, ensuring compliance with GLP/GMP, and fostering innovation in product development.

Education: Pharm-D

Experience: Minimum of 5 years in R&D within the pharmaceutical industry

Responsibilities:

• Assist in the formulation and development of pharmaceutical products, including product stability studies and process optimization.
• Collaborate with cross-functional teams such as Quality Control, Regulatory Affairs, and Manufacturing to ensure efficient project execution.
• Conduct experiments for product development and support the evaluation of product safety, efficacy, and stability.
• Prepare technical documentation, reports, and presentations related to research outcomes and project status.
• Support troubleshooting and problem-solving efforts in R&D processes.
• Stay updated with advancements in pharmaceutical science and recommend improvements for product innovation.
• Ensure laboratory activities comply with Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP) standards.

• Proven experience in pharmaceutical formulation and development processes.
• Familiarity with regulatory requirements for pharmaceutical product development.
• Strong analytical and problem-solving skills.
• Ability to manage multiple tasks effectively and meet deadlines.
• Knowledge of novel drug delivery systems or biologics is an added advantage.

Job Type: Full-time

Genetics Pharmaceuticals Pvt Ltd, Pakistan

Responsible for quality assurance for secondary manufacturing/formulations

To continuously review quality control processes, procedures and capabilities in order to sustain the most cost effective and efficient methods for meeting quality requirements, and making recommendation for improvement as appropriate.

Review client QC requirements and ensure that quality control documentation for a project meets requirements.

Review and approve Contractor and subcontractor quality control documentation to ensure their planned activities meet contractual requirements

To coordinate all activities required to direct and control manufacturing quality. In particular to review product quality requirements for individual clients and projects, to ensure those requirements are understood and implemented to manage the quality of manufactured items to meet the requirements of the contract specifications.

Manage and control all quality control activities in accordance with identified Quality Assurance standards, company procedures, client specifications and contract requirements.

Assist in production of generic and project specific Method Statements and Risk Assessments.

Achieves quality assurance operational objectives by contributing information and analysis to strategic plans and reviews; preparing and completing action plans; implementing production, productivity, quality, and customer-service standards; identifying and resolving problems; completing audits; determining system improvements; implementing change.

Meets quality assurance financial objectives by estimating requirements; preparing an annual budget; scheduling expenditures; analyzing variances; initiating corrective actions.

Develops quality assurance plans by conducting hazard analyses; identifying critical control points and preventive measures; establishing critical limits, monitoring procedures, corrective actions, and verification procedures; monitoring inventories.

Validates quality processes by establishing product specifications and quality attributes; measuring production; documenting evidence; determining operational and performance qualification; writing and updating quality assurance procedures.

Maintains and improves product quality by completing product, company, system, compliance, and surveillance audits; investigating customer complaints; collaborating with other members of management to develop new product and engineering designs, and manufacturing and training methods.

Prepares quality documentation and reports by collecting, analyzing and summarizing information and trends including failed processes, stability studies, recalls, corrective actions, and re-validations.

Updates job knowledge by studying trends in and developments in quality management; participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations.

Enhances department and organization reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments.

- Prepare for inspections based on work instructions.

- Conduct product quality inspections on-site according to schedules.

- Take photos of products, defects, packing, etc during the inspections.

- Draft the inspection reports and submit the reports to the head office within 12 hours after inspections.

Requirements:

- Intermediate graduate or above.

- More than 2 years experience in garment / shoes / home textile / furniture / engineering inspections.

- Familiar with AQL standards and good knowledge of safety and regulation standards.

- Good command of written & oral English.

- Good interpersonal and communication skills.

Information Technology and Services - Guangzhou, China

Job specifications are given below:

1. Responsible for regulatory requirements and their interpretation such as Current Good Manufacturing Practices, Good Laboratory practices, Equipment purchase, calibration, repair and Maintenance, Stability Guidelines, Validation, Cleaning Validation, Facilities, and other requirements as they relate to the production processes, Product Development and Modification, In-process Control systems, complaint Handling, Packaging Engineering and Operations, identifying trends, recommendations for system improvement, Supplier Evaluation, Annual Contracts with the Suppliers, Use of statistical techniques for Data Analysis.
2. Responsible for Quality Planning, Organize, Direct, Control and Evaluate the activities related to the Quality.
3. Responsible for Quality Operations, Budgeting, Goal Setting of Quality Assurance Department.
4. Responsible to consult and negotiate with equipment vendors and suppliers to prepare specifications, explain proposals and present the Quality Reports and findings.
5. Responsible to assign, co-ordinate and review the Technical Work of the Department or project team.
6. Responsible for Recruit Personnel, Development and maintenance of staff competence in required area, Training and accomplishment of Technical Resources with a proven record in building and motivation of Quality Assurance Efforts.
7. Accomplishes staff results by communicating job expectations, planning, monitoring, and appraising job results, coaching, counseling, and disciplining staff, developing, coordinating, and enforcing systems, policies, procedures, and productivity standards.
8. Responsible to investigate system problems in order to recommend and implement solutions.
9. To establish and operate change control system to assurance compliance for the facility, equipment, processes and acceptance limits.
10. Responsible to handle the Quality Affairs of Toll Manufacturing.
11. Responsible to control the laboratory operations of the Micronutrient laboratory.
12. Responsible for research and development of new products comprising the Registration dossier, Material selections (Local and Import), Recipe Development, Trials preparation and their stability studies.
13. Responsible to execute the New Developed recipes at plant for Bulk Production.
14. Responsible for Modification and maintenance of existing formulations regarding the Quality Issues and economical aspects.
15. Responsible for the Formulations of the new products for different dosage forms of Pesticides, Especially EC, EW, OD, FS, SC, WP, WDG, WSG, WS, SP, SE, CF and SL etc.
16. Monitoring of all activities regarding new recipe development micronutrient products.
17. Responsible for development of analytical methods of Raw Materials, In process and finished Products.
18. Responsible for the Packaging Material Specification of all packaging components.
19. Responsible for Trainings of QA and plant staff.
20. Should have the strong knowledge and implementation skill as MR of International certification like ISO 9001:2008, 17025, 14000, OHSAS, EPA and others.
21. Responsible for the compliance of QMS, GMP and Regulatory audits.