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Product Quality Manager External Quality - QUA008497-



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Introductie



Het bedrijf / The company

MSD is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us. Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you"ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.

Our employees are the key to our company"s success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Our Company"s benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

De functie / The role

Are you ready for your next challenge in QA?


At MSD we have an exciting opportunity for a:





Product Quality Manager External Quality




As Product Quality Manager External Quality you are responsible for ensuring that all MSD products managed by EQA are manufactured, packaged, analyzed, released stored and distributed in accordance with MSD expectations and all applicable regulatory requirements. You ensure the Quality performance of external parties/partners through direct oversight, support and counselling to the partner. These activities include involvement in most aspects of external manufacturing operations related to the quality of products produced. You are responsible for the release of all manufactured products and to assure they have been produced from approved processes in conformance to all applicable regulatory requirements and Company policies. You exercise a leadership role in monitoring and maintaining the ExM compliance with the FDC Act, Current Good Manufacturing Practices Regulations (domestic and foreign) and other pertinent legal requirements




Main responsibilities
Reporting to the Director External Manufacturing, the Product Quality Manager External Quality works in a team of 4 and has the following responsibilities:

Assures compliance with established policies/procedures of the Division and Corporation and complies with all applicable governmental regulations (GMP, etc.), both domestic and foreign
Operates in a safe and efficient manner and in compliance with our Manufacturing Division QO Safety and Health Policy.
Supports ESQL with the development and maintenance of a Quality Agreement with the external parties/partners. May provide input into the development of contractual agreements with the external manufacturers.
Reviews all audit outcomes pertaining to external manufacturers and ensures appropriate and timely corrective actions were warranted.
Responsible for coordination, oversight, and communication on matters related to the GMP status of the external manufacturer. Must be conversant with applicable regulations and compendia (domestic and foreign) governing the external party/partner"s operations.
Closely collaborates with appropriate business/operations and technical areas to achieve MSD objectives.
Acts as the MSD Product Quality point of contact for the external party/partner and the liaison for contact and communications between the external party/partner and internal MSD personnel supporting the ESQL role.
Exercises a program of calibrated Quality oversight based on the product type, capabilities, and quality and compliance performance of the external party/partner. Tracks and monitors operational and quality performance of the external party/partner. Monitors efforts to improve the external manufacturer"s quality and reliability through ongoing oversight and formal communication programs and forums.
Works with the external party/partner to ensure that effective and robust Quality systems and Quality management are in place. Provides on-site guidance in the preparation of metrics, procedures, and guidelines where warranted. Provides proactive support in training and coaching to initate quality improvements.
Provides guidance to the partner on conducting investigations of batch rejection, atypical events, customer complaints, etc. where warranted.
Responsible for evaluation and/or release of products to other sites and/or to the market with the assurance that the goods were produced in conformance to all applicable policies/procedures of MSD and compliance with all governing regulations.
Leads the responding to complaints from domestic and international markets.
Ensures that all deviations at external manufacturer/partners related to MSD Products are fully investigated with any assigned actions effectively implemented within the agreed time frame.
Provides proactive support in training and coaching to initiate quality improvements within Operations and Quality; reviews Annual Product Stability and Annual Product Reviews
Creating and managing routine and/or compendial change control

Het profiel / Your profile

Qualifications
BS degree in Biology, Microbiology, Pharmacy, Chemistry, Chemical Engineering or equivalent.
Minimum of 5 years" experience in pharmaceutical industry with a thorough knowledge of quality systems, regulatory requirements and GMP.
Must have strong knowledge of and broad experience in product Quality Assurance and Quality Control activities.
Must have strong demonstrated interpersonal, communication, negotiation, and persuasion skills.
Fluent in English and Portuguese or Spanish.
Must have very strong relationship building skills.
Some level of contractual and financial awareness is required.
Qualified Person according to Article 48 of Directive 2001/83/EC (preferred not required)
Willingness to travel up to 25%, mostly to Lisbon.

Het aanbod / The offer

What we offer
We welcome you to a truly global, dynamic and challenging environment with great opportunities for personal development. Our benefits are very competitive.

Reactie / Reaction

Application
If you are interested in this challenging role, you are invited to apply online by uploading your resume and application letter in English.

Tenslotte ..... / Finally ....


Search Firm Representatives Please Read Carefully:
MSD is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at MSD via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of MSD. No fee will be paid in the event the candidate is hired by MSD as a result of the referral or through other means. #LI-DNI


Solliciteer hier
Indien solliciteer hier u verwijst naar een ongeldig webadres, is de vacature (hoogstwaarschijnlijk) inmiddels vervuld. Attendeer FMF hierop

Uw referentie aan www.fmfvacatures.nl wordt gewaardeerd.
Your referral to www.fmfvacatures.nl is appreciated.


Gegevens

Werkgever:
MSD
Vacaturesteller:
Barbara Razenberg
Standplaats:
Haarlem

Geplaatst op FMF: 22 januari 2019

Branche: Farma & Biotech, Medical, Healthcare
Functie: QA / regulatory, QC / Laboratory, Produktie/Engineering/Facility, Planning & Logistiek
Opleidingsniveau: HBO / BSc, WO/academisch / MSc, PhD
Werkervaring: 5-10 jaar, > 10 jaar