the team's size and operational scope. Key qualifications: Extensive experience in Quality Assurance across diverse responsibilities Preferably, a background in pharmaceuticals, though other GMP environments will be considered Bachelor's degree or equivalent in a relevant technical field Strong proficiency across various quality functions such as batch review, investigations … into a senior leadership role within a fast-paced pharmaceutical environment, apply now to become part of a dedicated team. Keywords: Quality, QA, assurance, GMP, manufacturing, distribution, packaging, CDMO, pharmaceutical, batch release, systems, compliance, regulatory, specialist, investigations, CAPA, deviation, change control, operations, senior, leader, supervisor, manager, coach, mentor. more »
product Additional Skills & Qualifications: • Minimum 3 years of experience in Quality within a laboratory environment, preferably food/beverage industry • Knowledge of quality systems (GMP, HACCP, SQF) About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and more »
/equivalent vocational training and/or have equivalent time served experience within a Quality, Scientific or Engineering environment. Awareness of working in a GMP environment Ability to communicate with all areas of an organisation Perform work in compliance with established procedures Understanding of computer software including Word, Excel and more »
and on occasions as required If you would like to discuss this further, please contact Mark Bux-Ryan for further information. QP, qualified, person, GMP, manufacturing, sterile, terminally, sterility, aseptic, quality, assurance, manager, leader, MHRA, audit, release more »
and on occasions as required If you would like to discuss this further, please contact Mark Bux-Ryan for further information. QP, qualified, person, GMP, manufacturing, sterile, terminally, sterility, aseptic, quality, assurance, manager, leader, MHRA, audit, release more »
and on occasions as required If you would like to discuss this further, please contact Mark Bux-Ryan for further information. QP, qualified, person, GMP, manufacturing, sterile, terminally, sterility, aseptic, quality, assurance, manager, leader, MHRA, audit, release more »
Market Drayton, Shropshire, West Midlands, United Kingdom
Muller Dairy
and provide corrective action Use root cause analysis to understand and deliver optimal cost maintenance Delivery of the required standards in relation to Engineering GMP and food safety standards Escalate potential consequences to line manager where work may impact on product quality or safety Key skills & experience: Strong engineering qualifications more »
out by all departments. ·Conduct shelf-life trials and record results accurately. ·To ensure equipment is calibrated and checked as per schedule. ·To complete GMP, glass and internal audits as required. ·To work closely with the intake team on raw material, packaging and label receipt and ensure any non-conformances more »
methods. • Follows and complies with all safety and work rules and regulations. Maintains departmental housekeeping standards. • Other duties as assigned. Skills: Quality control, Laboratory, Gmp, Quality assurance, Qc Additional Skills & Qualifications: QUALIFICATIONS: Education and Experience • 3-5 years related experience and or/training; or equivalent combination of education and more »
from a Pensions background and ideally Team Leading people working on similar projects as listed below. - Pensions Data Transfer - Client Onboarding - Implementation - System Configuration - GMP - BIBO - Buy in - Buy out - Pension projects Unique culture, fully diverse and inclusive, very supportive, with ability to grow and become senior manager. Responsibilities: Takes more »
Skills: Experience working with fragrance and/or flavors is a must. Bachelor's degree in the sciences is preferred. Experience working within a GMP regulated environment. Why work here? They are a global purpose-led, science-based company specializing in Nutrition, Health & Sustainable Living. Their purpose is to create more »
and improvement of the Quality Management System (QMS). Assure the compliance of all activities with Good Distribution Practice (GDP) and GoodManufacturingpractice (GMP) requirements. Responding to medical information enquiries from healthcare professionals, community pharmacies, patients, and wholesalers. Ensuring the completion of checks for new products; having the appropriate more »
planning, resource and cost management and progress reporting. Your background - experience gained within the pharmaceutical industry - experience of ensuring compliance with all EHS and GMP requirements - experience of writing SOP's - formal engineering qualification - preparation of pre-qualification document for new and retrospective projects -flexibility to travel to alternative sites more »
Lead best practice in the department and become a key contact for the mentoring and training of more junior members of staff. Act as GMP ambassador, take responsibility for ensuring GMP compliance and adoption of GMP principles e.g., right first time. Lead activities to ensure close working with Analytical development … understanding of cell biology and immunology (preferred) Strong verbal and written communication skills. Flexible, self-motivated, and focused on team outcomes. Strong understanding of GMP regulations. Excellent organisational skills with the ability to present results clearly and logically, working co-operatively as part of a team, as well as independently. more »
analytical team to contribute to the overall group objectives and development of staff. Ensure that own work, and that of the team, complies with GMP, Good Documentation Practice (GDP) and GxP Data Integrity guidance's, and is undertaken in accordance with applicable procedures (e.g., SOP's, Protocols, etc). Requirements … Proven track record of managing a team within a cGMP QC analytical environment. Degree in a relevant scientific discipline or equivalent experience. Understanding of GMP requirements e.g. legislation, guidelines and requirements related to Gene Therapy, QC method qualification and validation, QC processes, equipment and systems, including Computer System e.g. of … EU GMP requirements for Advanced Therapy Medicinal Products, EU/FDA GMP guidelines, EU Annex 1, EU Annex 11 & CFR Part 11 and ICH guidelines Q1-Q10. Apply now If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy more »
the company schedule. Qualifications: Experience in Food/Beverage Laboratory preferred. Minimum of 3 years of experience in a quality lab setting. Knowledge of GMP, HACCP and SQF (certification ideal). Why work here? Medical/dental/vision insurance Life insurance 401(k) savings plan with company match Paid more »
with regulatory agencies during inspections. Skills: analytical chemistry, method validation, HPLC, UPLC, tech transfer, quality assurance, deviation Qualifications: •10 years of experience in a GMP environment-related field (analytical laboratory experience, specifically method development or method validation) and a BS or BA. • 3+ years of relevant experience (analytical laboratory experience … Whys). • Working knowledge of Risk Management Tools (e.g., root cause analysis, decision trees, risk registers). • Experience in a Pharma/Biotech GMP environment and a bachelor's degree in chemistry, biology, or related scientific fields. • Expertise in Quality Systems and cGMP standards applicable to method validation for clinical more »
qualifications and experience: 5 years experience in an environment associated with the manufacture, testing, and dispensing of radiotracers. Relevant experience of GoodManufacturingPractice (GMP), typically 2 years post qualification. Experience of working in Radiotracer production facility, Aseptic service or similar environment. Experience supervising technical staff and management of resources. more »
of working within a Quality Assurance Officer role within a fast-paced environment. You should have at least 2 years' experience of working under GMP or have a degree within a science discipline. Knowledge and understanding of GMP with excellent communication and organisation skills are essential for this role. To … Society, Royal Society of Chemistry or Institute of Biology, GPhC, Science Council. Your duties & responsibilities The final review of pre-manufacture batch documentation, following GMP guidelines. The Approval for Use (final release) of all products manufactured or repackaged according to licensing requirements, GMP and professional discretion Being the primary point … attend any suitable training and update courses as deemed necessary and ensure a high level of competency is achieved. Ensuring that staff comply with GMP, COSHH and Health and Safety regulations and departmental SOP's. Participating in any rota system that may operate within the product release team in order more »
and maintenance of the company's Quality Management System (QMS) in accordance with regulatory requirements. Assist in conducting internal audits to assess compliance with GMP/GDP standards and company policies. Participate in the review and approval of GMP documentation, including batch records, SOPs, and change controls. Assist in deviation … Bachelor's degree in Pharmacy, Chemistry, or related field. Some experience or internship in a pharmaceutical quality assurance role is preferred. Basic knowledge of GMP/GDP regulations and quality management systems. Strong analytical and problem-solving skills, with attention to detail. Effective communication and interpersonal skills. Ability to work more »
the laboratory function in executing daily operations and testing necessary to support commercial products. • Anticipates and resolves problems independently while conforming to SOPs and GMP regulations • Monitors the scientific and financial progress of projects that they are assigned • May have responsibility for a laboratory group or function and may have … timely manner and are completed within established target completion dates o Ensure that the Quality Control staff have been appropriately trained before performing a GMP task 3. Productivity o Serve as primary resource for planning and scheduling of tests o Assist analysts as needed and troubleshoot if required o Witness … and organizational skills o Ability to work with a sense of urgency in a fast-paced environment o Strong technical writing and investigational skills GMP DECISION-MAKING AUTHORITY The Team Leader Quality Control is responsible for decisions related to: o When an investigation is warranted o When analyst training is more »
Hoddesdon, Hertfordshire, South East, United Kingdom
PHARMARON UK LIMITED
focused Extremely safety conscious Helpful and responsive and committed to delivering the very best Team playing whilst proactive and a self-starter Desirable Requirements: GMPmanufacturing equipment Recognised formal qualification in secondary control discipline or equivalent experience in Control Systems Knowledge of high integrity PCS and PLC programming would be … Drug Discovery teams. In addition, a Formulation Development team was also recently established. The Hoddesdon site has state-of-the-art GoodManufacturingPractice (GMP) standard facilities for the development of Active Pharmaceutical Ingredients (API), Formulation Development (FD) and Process Chemistry (PC). We offer a competitive salary and a more »
East Kent Hospitals University NHS Foundation Trust
risk assessments Experience of participating in audits/internal monitoring Desirable Knowledge of regulatory requirements relating to clinical trials Awareness of GoodManufacturingPractice (GMP) inc Annex 13 labelling requirements Personal/Professional attributes Essential Excellent attention to detail. High level of initiative Able to problem solve Able to work more »
of pharmacist as required3.Participation in screening, dispensing and checking of clinical trial prescriptions, and advising others of Good Clinical Practice (GCP), GoodManufacturingPractice (GMP) and requirements relating to Investigational Medicinal Product (IMP) management.4.To participate in the Trust-wide Out of Hours Medicines Advice Service and seven-day medicine supply more »
