Search Results: 10,638 vacancies
...directly for a Middlesex County, NJ area company that develops solutions for the beauty industry.
Quality Manager:
Job Purpose:
To direct and administer all Regulatory Affairs, permits, filings and training including Global Compliance. Develop, implement and...
Suggested
...Job Title: Quality Manager
Job Location: New Brunswick, NJ
Job Duration: 12+ Months
Job Description:
Provides Quality... ...Food and Drug Administration (FDA) and international regulatory standards. In addition, this position has responsibility to...
Suggested
Contract work
Remote job
...Job Title: Quality Manager
Duration: 12 months
Location: New Brunswick NJ 08903
Comments: 100% onsite , Bachelor degree required... ...Food and Drug Administration (FDA) and international regulatory standards. In addition, this position has responsibility to...
Suggested
Contract work
Remote job
...Job title: CMC Regulatory Technical Writer II
Location: Bridgewater, NJ, Hybrid... ...Regulatory Technical Writer II authors high quality Module 2 and 3 regulatory submissions for... ...documents for meetings).
He/she defines and manages the compilation of the documentation,...
Suggested
Contract work
Shift work
Day shift
...innovative and highly motivated individual to join us as the Manager, Quality Control Microbiology at our GMP manufacturing facility... ...dossiers and data packages in support of Cellares products for regulatory agencies
Manage and grow a phase appropriate team of Quality...
Suggested
Contract work
Flexible hours
...distribution, control panels, and power cable assemblies. Due to our rapid growth and expansion, we are seeking an experienced Quality Control Manager to support and expand our commitment to excellence and maintain our goal of total customer satisfaction.
As a Quality...
Suggested
Work experience placement
...Lead the development and execution of regulatory strategies for PMA submissions, ensuring... ...submission to post-approval activities.
Manage interactions with regulatory agencies... ...communications.
Establish and maintain a robust quality management system (QMS) to support PMA...
Suggested
...Breckenridge Pharmaceutical develops and markets high-quality, added-value and cost-effective generic drugs in the United States. Our... ...reports to the Associate Vice President, Quality Assurance and will manage or support: cGMP compliance assessment of contract...
Suggested
Contract work
...We are currently seeking a Global Regulatory Affairs Lead (GRL) who will be the fully accountable decision maker for the development &... ...core product labeling in development as well as for life cycle management within our Immunology therapeutic portfolio
Responsible for...
Suggested
...manufacturing facilities, we provide high-quality, affordable medicines, trusted by... ...OF CONDUCT
This position shall ensure regulatory compliance of all Sun sites, with products... ...America Compliance activities, as needed.
* Management of Field Alert Repots (FARs) including...
Suggested
Temporary work
Local area
Immediate start
Overseas
Flexible hours
...Responsibilities:
Provides administrative support for regulatory affairs manager
Provides RA support for change control projects and... ...evaluation skills US FDA medical device regulations, standards, and guidance
21 CFR 820 - Quality System Regulation....
Suggested
Worldwide
...applicable laws and regulations.
Responsibilities:
* Provides regulatory review and approval of advertising and promotional materials,... ...products.
* Strong organizational skills and excellent in managing multiple priorities.
* Excellent communication skills (oral...
Suggested
Holiday work
Fixed term contract
Remote job
Work visa
...healthcare and serve as a leader of positive change.
The Regulatory Specialist is responsible for promoting compliance with Federal... ...terminology.
Ability to work in a fast-paced environment and manage competing tasks and demands.
Licenses and Certifications...
Suggested
Local area
...position is responsible for the preparation of regulatory submissions required to market medical... ...registration information with R&D, Quality, Medical, Manufacturing, etc.
Assess... ...Strong communication and project management skills
Must be able to handle multiple...
Suggested
...Responsibilities:
Develop global regulatory strategies for medical device products to meet business objectives and... ...clearance, approval, and continuance during product life cycle management that includes (but is not limited to) 510(k)s, PM, De Novo, and...
Suggested
About the job Food Safety Quality Assurance Manager
Responsibilities:
Oversee the operations of microbiology and chemistry laboratories, including managing personnel and programs.
Assist in enhancing and periodically reviewing the facility's food safety and...
...over 40 years.
Overview:
The Site Quality Leader is responsible to lead the... ...exceeds customer expectations, satisfies regulatory requirements, improves operational efficiency... ...and high technical integrity.
Manage the performance of the team through key...
Holiday work
...Director of Advertising and Promotion, Prescription Drug Products manages and/or participates in the review, approval and monitoring of... ...are in compliance with all applicable laws, regulations, and regulatory agency guidance.
**KEY ACTIVITIES/RESPONSIBILITIES:**
+...
Holiday work
Temporary work
Flexible hours
...health in the future.
**Objectives/Purpose of Job:**
+ The Regulatory Affairs Senior Specialist handles US regulatory development aspects... ...support marketed OTC monograph/NDA or cosmetic products.
+ Manages relevant regulatory strategy components and interactions with...
Work visa
...Description We have an awesome opportunity for an experienced Quality Manager to join a $1B International Specialty Chemical Manufacturing... ...its quality registrations e.g. ISO 9000; passes all regulatory and customer audits; and ensures the site meets cGMP and IPEC...