8 Remote Pharmaceutical Quality Control Specialist jobs in whatjobs
Remote Pharmaceutical Quality Control Specialist
Posted 21 days ago
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Remote Pharmaceutical Quality Control Specialist
Posted 13 days ago
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Responsibilities:
- Perform comprehensive quality control testing on raw materials, in-process samples, and finished pharmaceutical products.
- Operate and maintain analytical laboratory equipment, ensuring calibration and performance.
- Analyze test results, interpret data, and generate reports, ensuring accuracy and completeness.
- Review and approve batch manufacturing records and analytical documentation.
- Investigate deviations, out-of-specification (OOS) results, and product complaints, implementing CAPAs.
- Ensure all quality control activities comply with GMP, GLP, and other regulatory requirements.
- Assist in the validation of analytical methods and equipment.
- Contribute to continuous improvement initiatives within the quality control department.
- Maintain accurate and organized laboratory records and databases.
- Stay updated on pharmaceutical quality standards and regulatory changes.
Qualifications:
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific discipline.
- Proven experience in pharmaceutical quality control or quality assurance roles.
- Strong knowledge of GMP, GLP, and relevant pharmaceutical regulations.
- Hands-on experience with analytical techniques such as HPLC, GC, spectroscopy, and dissolution testing.
- Proficiency in statistical analysis and data interpretation.
- Excellent documentation skills and meticulous attention to detail.
- Ability to work independently, manage time effectively, and meet deadlines in a remote environment.
- Strong problem-solving and critical thinking abilities.
- Familiarity with LIMS (Laboratory Information Management System) is a plus.
Remote Pharmaceutical Quality Control Specialist
Posted 13 days ago
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Remote Pharmaceutical Quality Control Specialist
Posted 19 days ago
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Remote Pharmaceutical Quality Control Specialist
Posted 7 days ago
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Responsibilities:
- Review and approve batch manufacturing records (BMRs) and batch packaging records (BPRs) for compliance with cGMP.
- Perform in-depth analysis of quality control data, including analytical test results, stability data, and validation reports.
- Investigate deviations, Out-of-Specification (OOS) results, and customer complaints, identifying root causes and recommending corrective and preventive actions (CAPAs).
- Contribute to the development, validation, and implementation of analytical test methods.
- Participate in internal and external audits, ensuring readiness and compliance.
- Maintain and update quality documentation, including Standard Operating Procedures (SOPs), specifications, and change controls.
- Monitor and ensure compliance with relevant regulatory requirements (e.g., FDA, EMA, local Kenyan regulations).
- Collaborate with R&D, Manufacturing, and Regulatory Affairs departments to resolve quality issues.
- Assist in the qualification and monitoring of raw material suppliers and contract manufacturing organizations.
- Support continuous improvement initiatives within the quality control department.
- Ensure all activities are documented accurately and in a timely manner.
- Bachelor's degree in Pharmacy, Chemistry, Biotechnology, or a related life science field.
- Minimum of 3 years of experience in pharmaceutical quality control or quality assurance.
- In-depth knowledge of current Good Manufacturing Practices (cGMP) and other relevant pharmaceutical regulations.
- Experience with analytical techniques such as HPLC, GC, spectroscopy, and dissolution testing.
- Strong understanding of quality management systems and documentation control.
- Excellent attention to detail, accuracy, and organizational skills.
- Proficiency in data analysis and interpretation.
- Effective written and verbal communication skills, with the ability to present technical information clearly.
- Ability to work independently, manage multiple tasks, and meet deadlines in a remote work environment.
- Familiarity with pharmaceutical product lifecycle and development is advantageous.
- This remote position will support the company's operations impacting the region around Mlolongo, Machakos, KE .
Remote Pharmaceutical Quality Control Specialist
Posted 7 days ago
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Remote Pharmaceutical Quality Control Specialist
Posted 2 days ago
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Responsibilities:
- Develop and implement quality control procedures for pharmaceutical products.
- Review and analyze analytical test data from raw materials, in-process samples, and finished products.
- Ensure compliance with Good Manufacturing Practices (GMP) and other relevant regulations.
- Investigate deviations, out-of-specification results, and out-of-trend data.
- Participate in internal and external audits of manufacturing processes and suppliers.
- Prepare and review quality control documentation, including SOPs and batch records.
- Collaborate with R&D, manufacturing, and regulatory affairs teams on quality-related matters.
- Monitor and report on key quality control metrics.
- Contribute to the continuous improvement of quality systems.
- Stay updated on pharmaceutical quality control best practices and regulatory changes.
Qualifications:
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field.
- Minimum of 5 years of experience in pharmaceutical quality control or quality assurance.
- In-depth knowledge of GMP guidelines and regulatory requirements for pharmaceuticals.
- Strong understanding of analytical testing methods (e.g., HPLC, GC, spectroscopy).
- Proven experience in investigating deviations and implementing corrective/preventive actions (CAPA).
- Excellent attention to detail and organizational skills.
- Strong written and verbal communication skills for technical documentation and reporting.
- Demonstrated ability to work independently and manage tasks effectively in a remote setting.
- Proficiency with quality management software and standard office applications.
- Experience with validation protocols is a plus.
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Remote Pharmaceutical Quality Control Specialist
Posted 2 days ago
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Responsibilities:
- Conduct analytical tests on pharmaceutical samples using various laboratory techniques and instrumentation (e.g., HPLC, GC, UV-Vis spectroscopy).
- Evaluate test results against established specifications and regulatory guidelines (e.g., GMP, pharmacopeias).
- Maintain accurate and detailed laboratory records, documenting all procedures, results, and deviations.
- Prepare reagents, solutions, and standards required for testing.
- Calibrate and maintain laboratory equipment to ensure accuracy and reliability.
- Participate in method validation and transfer activities.
- Investigate out-of-specification (OOS) results and implement corrective and preventive actions (CAPAs).
- Review batch records and other quality-related documentation.
- Stay updated on current Good Manufacturing Practices (cGMP) and relevant regulatory requirements.
- Collaborate with other departments, including R&D, Manufacturing, and Quality Assurance, to resolve quality issues.
- Bachelor's degree in Chemistry, Pharmacy, Biotechnology, or a related scientific discipline.
- Minimum of 4 years of experience in pharmaceutical quality control or quality assurance.
- Proficiency in analytical techniques commonly used in pharmaceutical testing, such as HPLC, GC, dissolution testing, and spectroscopy.
- Familiarity with cGMP, ICH guidelines, and relevant pharmacopeias (e.g., USP, EP).
- Experience with laboratory information management systems (LIMS) is a plus.
- Strong analytical, problem-solving, and critical-thinking skills.
- Excellent attention to detail and accuracy in data recording and reporting.
- Effective written and verbal communication skills, particularly for documenting findings and collaborating remotely.
- Ability to work independently and manage workload effectively in a remote setting.
- Experience with sterile product testing or microbiology is an advantage.