-
Associate Director, GMP Quality Control
4 days ago
Sumitomo Pharma Trenton, United StatesSumitomo Pharma America (SMPA) is focused on delivering therapeutic and scientific breakthroughs in areas of critical patient need spanning psychiatry & neurology, oncology, urology, women's health, rare disease, and cell & gene therapies. The company's diverse portfolio includes ...
-
Director of GMP Quality Assurance
2 days ago
Madrigal Pharmaceuticals Conshohocken, PA, United StatesThis position will be responsible for Quality Assurance oversight of all analytical aspects. The primary responsibilities will be to ensure quality and accuracy of analytical data and compliance to approved methods and regulatory filings. This position will participate in technol ...
-
Director of GMP Quality Assurance
3 days ago
Madrigal Pharmaceuticals Inc Conshohocken, United StatesThis position will be responsible for Quality Assurance oversight of all analytical aspects. The primary responsibilities will be to ensure quality and accuracy of analytical data and compliance to approved methods and regulatory filings. This position will participate in technol ...
-
Director of GMP Quality Assurance
3 days ago
Madrigalpharma Conshohocken, United StatesThis position will be responsible for Quality Assurance oversight of all analytical aspects. The primary responsibilities will be to ensure quality and accuracy of analytical data and compliance to approved methods and regulatory filings. This position will participate in technol ...
-
Associate Director, Quality Assurance
4 days ago
J-STAR Research Trenton, United StatesPrerequisites · ≥ 7 years of experience within the pharmaceutical/biotechnology industry or CDMO industry is required. · ≥ 3 years of experience in small molecule cGMP processing, analysis and/or release testing is required. · ≥ 3 years of experience in process chemistry is pr ...
-
Director, Plant Operations
21 hours ago
Promotion In Motion Trenton, United StatesDo you love candy and snacks? Are you looking to join an ever evolving and rapidly growing team? PIM Brands might just be exactly what you're looking for · At PIM, we make the brands you love. Our portfolio of products, from Welch's Fruit Snacks to Sun-Maid Chocolate Raisins and ...
-
Director Production
2 days ago
Irving Knight Group Trenton, United StatesJob Title: · Dry Blend Director · Work Location: · New Jersey · Overview: · The Dry Blend Director is responsible for managing the dry blending production process. While the Director will work under the direction of the Dry Blend Vice President, he/she will serve as the back ...
-
Director, Plant Operations
2 days ago
PIM Brands , LLC Defunct Trenton, United StatesJob Details · Job Location · Somerset - Somerset, NJ · Position Type · Full Time · Education Level · 4 Year Degree · Job Shift · All Shifts (1st, 2nd & 3rd) · Job Category · Management · Description · Do you love candy and snacks? Are you looking to join an ever evolving a ...
-
TCG GreenChem Inc. Trenton, United StatesAssociate Director, Process Chemistry Kilo Lab (PCKL) · Job Summary · Responsible for contributions to the scale up of APIs under non-GMP and cGMP manufacturing in the Process Chemistry Kilo Lab (PCKL). This position requires responsibility of delivery of all required drug subst ...
-
Perspective Therapeutics, Inc Trenton, United StatesObjective · The Site Leader, Radiopharmaceutical Manufacturing is responsible for leading and managing site operations involved in the production of radiopharmaceuticals for both investigational and commercialization of drug products at the specified Perspective Therapeutics' pr ...
-
Senior Director
2 days ago
Enzene Biosciences Trenton, United StatesWe are looking for a Senior Director, Quality Assurance to lead our US Quality operations and ensure compliance with global regulatory standards and customer expectations. You will be responsible for overseeing the quality systems, processes, and personnel at our state-of-the-art ...
-
Director, CMC Operations
1 day ago
Perspective Therapeutics, Inc Trenton, United StatesObjective · The Director, CMC Operations responsible for technically designing, managing, and executing a plan for the use of alpha emitting Pb-203 & Pb-212 radiopharmaceuticals and the manufacturing of drug candidates supporting clinical trials and readiness for commercial deplo ...
-
Perspective Therapeutics Trenton, United StatesSite Leader, Radiopharmaceutical Manufacturing · Objective · The Site Leader, Radiopharmaceutical Manufacturing is responsible for leading and managing site operations involved in the production of radiopharmaceuticals for both investigational and commercialization of drug prod ...
-
Senior Manager, Contract
21 hours ago
Alvogen Emerging Market Holdings Limited Trenton, United StatesIf you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process. · Regular Full-Time · Manager · Morristown, NJ, US · 5 days ago · Requisition ID: 1930 · SUMMARY OF POSITION · We are lo ...
-
Senior CMC Project Manager
6 days ago
Genmab A/S Trenton, United StatesThe Genmab Vacancy Website is hosted by our Global HR System vendor, Workday. If you have any questions related to the hosting of this site please contact us at · . · Senior CMC Project Manager page is loaded · Senior CMC Project Manager · Apply · locations · Copenhagen · t ...
-
Director, Quality Assurance
1 day ago
Perspective Therapeutics Trenton, United StatesThe Director, Quality Assurance oversees Perspective Therapeutics' (PTX) Somerset, New Jersey Quality Management System (QMS) and ensures that the system and Somerset site operation are compliant with applicable regulations, standards and company requirements. This leader provide ...
-
Director, Quality Assurance
1 day ago
Perspective Therapeutics, Inc Trenton, United StatesThe Director, Quality Assurance oversees Perspective Therapeutics' (PTX) Somerset, New Jersey Quality Management System (QMS) and ensures that the system and Somerset site operation are compliant with applicable regulations, standards and company requirements. This leader provide ...
-
IT Site Shared Services
1 day ago
Bristol-Myers Squibb Trenton, United StatesIT Site Shared Services & Lab Systems Lead, Associate Director page is loaded · IT Site Shared Services & Lab Systems Lead, Associate Director · Apply · locations · Summit West - NJ - US · time type · Full time · posted on · Posted 9 Days Ago · job requisition id · R · ...
-
Analytical R
21 hours ago
Apozealpharma Levittown, United StatesAnalytical R & D/Quality Control Director · APOZEAL is a pharmaceutical company that is focused on the development and manufacturing of high-quality branded and generic pharmaceuticals across a broad range of therapeutic areas. · Title: · Analytical R & D/Quality Control Direct ...
-
Manager, GMP Quality Assurance
1 day ago
PMV Pharmaceuticals Inc Princeton, United States FreelanceManager, GMP Quality Assurance - Contractor · Reports to: Associate Director, GMP Quality Assurance · Location: Princeton, NJ, Hybrid · This contracting role is responsible for providing GMP QA expertise, oversight and auditing support of contract manufacturing organizations sup ...
Associate Director, QA GMP - Trenton, United States - Genmab A/S
Description
The Genmab Vacancy Website is hosted by our Global HR System vendor, Workday. If you have any questions related to the hosting of this site please contact us at.
Associate Director, QA GMP page is loaded
Associate Director, QA GMP
Apply
locations
Copenhagen
posted on
Posted 12 Days Ago
job requisition id
R10290
At Genmab, we're committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases.
From our people who are caring, candid, and impact-driven to our business, which is innovative and rooted in science, we believe that being proudly unique, determined to be our best, and authentic is essential to fulfilling our purpose.
The Role & DepartmentAt Genmab we are now looking to further strengthen the Late Stage Development QA Team located in Denmark. In this position, the Quality Assurance (QA) Associate Director will set the quality direction for Genmab's Late-Stage Development products.
As GMP QA Associate Director you will be an important part of the global GMP QA team to ensure compliance to industry standards and regulations.
This position will be located in DK, reporting to the Director of QA GMP Late-Stage Development (temporarily located in the US).
The role has no direct reports.The Global QA Department is composed of more than 50 employees working in GXP and are based in Denmark, the Netherlands, the US and Japan.
This role is located in Copenhagen, Denmark and is hybrid.Key responsibilities
Act as Delegated QP for the certification and release of IMP for clinical trials
Act as deputy RP for GDP processes and issues
Contributing to Quality Oversight of CMOs by auditing GMP and GDP CMOs, negotiating Quality Agreements, and performing vendor evaluations
Handling Product Complaints
Maintain training programs for GDP and GMP, train stakeholders in relevant GDP and GMP topics
Additionally, perform the following tasks as a part of the GMP QA Team
Maintaining and continuously improving Genmab's Pharmaceutical Quality System (PQS) to ensure compliance with GMP and GDP regulations
Reviewing and authoring of PQS SOPs, Work Instructions and documents
Gaining and maintaining knowledge on new/updated GMP/GDP-regulations and guidelines
Representing QA GMP in project groups to advise on GMP and GDP compliance
Promote collaborative relations with relevant internal stakeholders, partners, and CMOs
Handling of Deviations, CAPAs and Change Control in compliance with Genmab SOPs and applicable regulatory requirements
Participating in internal audits and audits and regulatory inspections performed by Partners, Health Authorities
Requirements
You hold a MSc degree or equivalent in a relevant life science subject
You have +10 years of experience from the pharmaceutical industry within QA preferably within biologics and/or sterile products and GDP
Experience within development products for clinical trials in late development phase including process validation is an advantage
Outsourcing experience, lead auditor experience is an advantage
Experience working in an EDMS system
You have excellent communication skills in English, and a collaborative mindset
As a person you enjoy an ambitious and changing environment
You are result and goal oriented and committed to contributing to the overall success of Genmab
About You
You are passionate about our purpose and genuinely care about our mission to transform the lives of patients through innovative cancer treatment
You bring rigor and excellence to all that you do. You are a fierce believer in our rooted-in-science approach to problem-solving
You are a generous collaborator who can work in teams with diverse backgrounds
You are determined to do and be your best and take pride in enabling the best work of others on the team
You are not afraid to grapple with the unknown and be innovative
You have experience working in a fast-growing, dynamic company (or a strong desire to)
You work hard and are not afraid to have a little fun while you do so
Locations
Genmab leverages the effectiveness of an agile working environment, when possible, for the betterment of employee work-life balance.
Our offices are designed as open, community-based spaces that work to connect employees while being immersed in our state-of-the-art laboratories.
Whether you're in one of our collaboratively designed office spaces or working remotely, we thrive on connecting with each other to innovate.
About GenmabGenmab is an international biotechnology company with a core purpose guiding its unstoppable team to strive towards improving the lives of patients through innovative and differentiated antibody therapeutics.
For more than 20 years, its passionate, innovative and collaborative team has invented next-generation antibody technology platforms and leveraged translational research and data sciences, which has resulted in a proprietary pipeline including bispecific T-cell engagers, next-generation immune checkpoint modulators, effector function enhanced antibodies and antibody-drug conjugates.
To help develop and deliver novel antibody therapies to patients, Genmab has formed 20+ strategic partnerships with biotechnology and pharmaceutical companies.
By 2030, Genmab's vision is to transform the lives of people with cancer and other serious diseases with Knock-Your-Socks-Off (KYSO) antibody medicines.
Established in 1999, Genmab is headquartered in Copenhagen, Denmark with locations in Utrecht, the Netherlands, Princeton, New Jersey, U.S. and Tokyo, Japan.Our commitment to diversity, equity, and inclusion
We are committed to fostering workplace diversity at all levels of the company and we believe it is essential for our continued success.
No applicant shall be discriminated against or treated unfairly because of their race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age, disability, or genetic information.
Learn more about our commitments on our website .Genmab is committed to protecting your personal data and privacy. Please see our privacy policy for handling your data in connection with your application on our website
.
Similar Jobs (1)
Associate Director, QA GCP/PV
locations
3 Locations
time type
Full time
posted on
Posted 26 Days Ago
Genmab is an international biotechnology company with a core purpose guiding its unstoppable team to strive towards improving the lives of patients through innovative and differentiated antibody therapeutics.
For more than 20 years, its passionate, innovative and collaborative team has invented next-generation antibody technology platforms and leveraged translational research and data sciences, which has resulted in a proprietary pipeline including bispecific T-cell engagers, next-generation immune checkpoint modulators, effector function enhanced antibodies and antibody-drug conjugates.
To help develop and deliver novel antibody therapies to patients, Genmab has formed 20+ strategic partnerships with biotechnology and pharmaceutical companies.
By 2030, Genmab's vision is to transform the lives of people with cancer and other serious diseases with Knock-Your-Socks-Off (KYSO) antibody medicines.
Established in 1999, Genmab is headquartered in Copenhagen, Denmark with locations in Utrecht, the Netherlands, Princeton, New Jersey, U.S. and Tokyo, Japan.#J-18808-Ljbffr