وظيفة في Cgmp في Munich

Job Title: CTM Associate (Clinical Trial Manufacturing) Length of Assignment: 12 months Shift/Schedule Details: Standard Business Hours MondayFriday 8am5pm Location: (Onsite) 100% Holly Springs NC 27540 Job Description: The CTM (Clinical Trial Manufacturing) Associate will be r المزيد...

Role and Responsibilities:As an Officer Production your primary responsibility will be to maintain workplacegood housekeeping as per cGMP standards and ensure the operation and cleaning of equipment as per SOP. You will be responsible for the receipt and storage of raw materials in t المزيد...

0-1 yrs experience with High School Diploma Ability to work independently or in collaboration with others on assigned tasks Ability to comply with cGMP standards Must possess computer skills Ability to follow instruction and directions Desirable Skills/Experience: المزيد...

Job Description: Overall incharge of Process Development Lab Activity. Solving/Guiding the entire QC related queries/problems inline with Quality Management System and the entire QC related problems to work consistently without any interruption. Responsible for المزيد...

إعداد ومراجعة إجراءات التشغيل القياسية المتعلقة بأنظمة الجودة باتباع الإرشادات الموضوعة وفقًا للوائح المصرية والمبادئ التوجيهية الموضوعة وفقًا لمتطلبات cGMP. إنشاء إجراء انحراف محدد ونظام CAPA، يشمل أصحاب المصلحة المناسبين للتحقيق والإغلاق. تجميع كافة المعلومات المتعلقة بالعمليات ا المزيد...

Primary Purpose / Regulatory Responsibilities: Establishment of robust fit for purpose biological drug product manufacturing processes for the different development phases (FIM Ph2 Ph3). Defining and selecting drug product manufacturing processes and parameters for clinical m المزيد...

Production Management: Oversee all aspects of production operations includingmanufacturing processes capacity planning scheduling and inventory management toensure timely and costeffective production of highquality pharmaceutical products incompliance with regulatory requireme المزيد...

Regulatory Affairs OfficerLocation: Delhi (Office Only)Experience: 25 YearsMustHave: USFDA Regulation 510(K) Compliance as per 21CFR 821. Coordinate with QC QA R&D MSAT Regulatory affairs teams on daytoday activities.Job Responsibility Responsible for product submis المزيد...

Analytical Engineer Manufacturing Support Location: Thousand Oaks CA Duration: 12 months (Possible extension) Key Responsibilities: Verification Leadership: Take individual accountability for verification deliverables on key capital projects. Assist in identifying critical qual المزيد...

Overview: TekWissen group is a workforce management provider throughout the USA and many other countries in the world. Our client is a leading biotechnology company that combines technological insight with worldclass manufacturing scientific expertise and process excellence and helps المزيد...

Independently plans and executes that support research, development and validation activities Support cGMP testing activities by performing analytical methods including UPLC/HPLC, Dissolution, GC, Thermogravimetric DSC/TGA, and KF titration. Perform data analysis and troubleshoot المزيد...

The successful candidate will be responsible for providing technical and/or engineering support for Finished Product (FP) manufacturing providing packaging engineering support through all phases of the commercial finished product lifecycle including technology transfer validation and المزيد...

Job Description: Bio Process Associate 3rd shift roleso shift diff included on Rate Onsite in DevensLocal Candidates Only Operates control systems and processes in Biotechnology Pilot Plants as assigned. Prepares process buffers and reagents. Cleans equipment and maintain area in cle المزيد...

Job Description: Primary Purpose SummaryThe Quality Control Technician performs dimensional and functional testing on Aptar Congers product to ensure compliance with established quality standards and customer specifications. The Quality Control Technician is responsible for documentin المزيد...

Lead Mechanic Westbury NY Full time/ Permanet/ 2nd shift: 3:00pm11:30pmWhat you will be doing:Responsible for machine related aspects such as packaging projects equipment maintenance parts and serviceReview daily mechanical activities to assure compliance with company cGMP s and SOP المزيد...

Full Knowledge of cGMP/GSDP guidelines Knowledge of national/international guidelines and references (FDA, EU, PICs, ICH, etc) Experience in writing and reviewing SOP's, systems, protocols , reports , etc. Experience in the quality management system (QMS) Experience in condu المزيد...

Job Responsibilities: Interfaces with Quality Assurance Production and Engineering departments on process requirements for new and current products. Equipment qualification including automation and computerized systems. Writes and executes evaluation protocols for all processing steps المزيد...

About PSC BiotechWho we arePSC Biotech is a leading Biotech Consultancy firm founded in 1996 headquartered in Pomona California USA with Global operations in Ireland India Singapore Australia and the US serving 350 clients in more than 23 countries worldwide. We provide cloudbased sof المزيد...

Job ProfilePlanning & Execution1. Planning for respective shifts and Execution of Warehouse activity2. Coordinate with different departments such as production QA QCDocumentation1. CGMP regulation in the warehouse department.2. Monitoring and Documentation of warehouse activities. المزيد...

The Packaging Operator is pivotal in the MDI product packaging process at the manufacturing site ensuring compliance with cGMP customer specifications and SOPs. They are tasked with executing packaging operations safely and efficiently to uphold product quality standards. This role ho المزيد...