SECTION 1: JOB SUMMARY Carry out QC testing to ensure the ongoing quality of product Interface with other departments to ensure timely release of products and materials Support with laboratory investigations and non-conformance investigations Ensure the principles of cGMP are applied and that all documentation is followed to comply with ISO9000, ISO13485, FDA QSRs and the Medical device directive Support documentation revisions SECTION 2: DUTIES & RESPONSIBILITIES Under supervision and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position involves: Ensure that QC testing is performed in a timely manner Day to day performance Physical testing of raw material, in process and finished product Analytical testing of raw material, in process and finished goods Chemical testing of raw material, in process and finished goods Management of consumables and materials used in testing Cleaning of items for testing within the laboratory Execution of the laboratory cleaning program Review of internal and external testing data Quality and Compliance Related Responsibilities Ensures that all activities are carried out in compliance with all regulations and laws governing business and quality operations Staff: Responsible for ensuring compliance with all local, national, international and company regulations, policies and procedures for Health, Safety and Environmental compliance. GMP documentation and Quality Systems Support investigations to assist in the completion of Non-conformance reports and OOS excursions Training Ensure that own training records are up to date and complete Assist in the training of other staff Validation Support validation of test methods and equipment for the QC department External communications Liaise with approved manufactures to ensure data is retrieved and available Ensure that consumables are ordered in a timely manner to avoid testing delays SECTION 3: EXPERIENCE AND EDUCATION Minimum of A level in science or mathematics discipline (international equivalents acceptable) Desired BSc degree in Scientific subject (Chemistry, Pharmacy, Forensics etc…) Minimum 1 years experience in a laboratory setting (Practical laboratory experience gained through a degree is acceptable) Working with Microsoft office applications (Word, Excel, PowerPoint, Office) Desired previous experience working within a quality environment in the Food, Consumer, Pharmaceutical or Medical device industry SECTION 4: REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES and AFFILIATIONS Able to follow procedures to ensure the principles of cGMP are upheld Able to communicate and present information and ideas effectively Able to work to deadlines Able to react to a changing environment and under time pressures Able to work as part of a team to work towards a common goal Able to manage own time and prioritize own workload to ensure timely completion of assigned work Credo values: Integrity and Credo based actions Customer focus: Results and Performance driven with a sense of Urgency Talent development: Collaboration, Self-awareness, Adaptability