5 Manufacturing Companies jobs in Deaf Hill

• Perform advanced analytical testing on raw materials, in-process samples, and finished pharmaceutical products using techniques such as HPLC, GC, UV-Vis, FTIR, and Karl Fischer titration.
• Develop, optimize, and validate analytical methods according to ICH guidelines and regulatory requirements.
• Analyze and interpret complex analytical data, generating comprehensive reports and documenting results accurately.
• Investigate out-of-specification (OOS) results, deviations, and non-conformances, identifying root causes and implementing corrective and preventative actions (CAPAs).
• Ensure all laboratory activities comply with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant regulatory standards.
• Maintain laboratory equipment, ensuring proper calibration, qualification, and maintenance.
• Participate in internal and external audits, providing necessary documentation and support.
• Contribute to the continuous improvement of quality control processes and laboratory operations.
• Stay updated on the latest scientific advancements, regulatory changes, and industry best practices in pharmaceutical quality control.
• Train and mentor junior QC analysts, providing guidance on testing procedures and data interpretation.
• Collaborate with R&D, manufacturing, and regulatory affairs teams to support product development and lifecycle management.
• Prepare and review technical documentation, including Standard Operating Procedures (SOPs) and validation protocols.

• Master's or Ph.D. in Pharmaceutical Sciences, Chemistry, Analytical Chemistry, or a related scientific discipline.
• Minimum of 5 years of hands-on experience in pharmaceutical quality control or analytical development.
• Extensive experience with various analytical techniques, particularly HPLC and GC, is essential.
• Strong understanding of GMP, ICH guidelines, and other relevant regulatory requirements.
• Proven ability to develop, validate, and transfer analytical methods.
• Excellent data analysis and interpretation skills, with meticulous attention to detail.
• Proficiency in LIMS (Laboratory Information Management System) and other relevant software.
• Strong written and verbal communication skills, with the ability to document findings clearly and concisely.
• Experience working remotely and managing laboratory operations or data analysis independently is a significant advantage.
• Ability to work effectively both independently and as part of a distributed team.

• Perform a wide range of analytical tests on raw materials, in-process samples, and finished pharmaceutical products using various sophisticated instruments (e.g., HPLC, GC, UV-Vis, IR spectroscopy).
• Develop, validate, and transfer analytical methods in accordance with ICH guidelines and regulatory requirements.
• Review and approve analytical data, ensuring accuracy, completeness, and compliance with established specifications.
• Troubleshoot and resolve analytical issues, instrument malfunctions, and out-of-specification (OOS) results.
• Maintain laboratory equipment, ensuring calibration, qualification, and preventative maintenance are performed regularly.
• Author and review analytical protocols, reports, and validation documents.
• Ensure all laboratory activities are conducted in strict adherence to Good Manufacturing Practices (GMP) and other relevant regulatory standards.
• Contribute to the maintenance and improvement of the Quality Management System (QMS).
• Participate in regulatory inspections and internal audits, providing necessary documentation and explanations.
• Assist in the investigation of deviations and implement corrective and preventive actions (CAPAs).
• Mentor and provide technical guidance to junior analysts.
• Stay abreast of advancements in pharmaceutical analysis, regulatory trends, and new technologies.
• Collaborate with R&D and manufacturing teams to support product development and process improvements.

• MSc or PhD in Analytical Chemistry, Pharmaceutical Sciences, Biochemistry, or a related scientific discipline.
• A minimum of 7 years of hands-on experience in pharmaceutical Quality Control or Analytical Development.
• Extensive experience with chromatographic techniques (HPLC, GC) and spectroscopic methods.
• Thorough understanding and practical application of GMP, ICH guidelines, and pharmacopoeial standards (e.g., USP, EP).
• Proven experience in method development and validation.
• Strong analytical, problem-solving, and critical thinking skills.
• Excellent written and verbal communication skills, with the ability to clearly document complex technical information.
• Proficiency in LIMS and other relevant laboratory software.
• Demonstrated ability to work independently and manage time effectively in a remote setting.
• Experience with stability testing programs.

Rewards and Benefits on Offer;

• Temp to Perm Opportunities available after a 6-month probation period
• Identified Manufacturing Career Path for progression including Industry lead training and development
• Leading Pay rates including higher overtime rates
• A well-regarded company culture
• Free on-site parking
• Excellent transportation links
• Recommend a Friend £50 gift voucher
• Christmas events and vouchers

The P.

WHJS1_UKTJ

Rewards and Benefits on Offer;

• Temp to Perm Opportunities available after a 6-month probation period
• Identified Manufacturing Career Path for progression including Industry lead training and development
• Leading Pay rates including higher overtime rates
• A well-regarded company culture
• Free on-site parking
• Excellent transportation links
• Recommend a Friend £50 gift voucher
• Christmas events and vouchers

The P.

WHJS1_UKTJ