What are the responsibilities and job description for the Specialist, Regulatory Science – Individual Contributor position at Actalent?
Description
****ONSITE**** Position Overview: Support manufacturing of orthopedic medical device products pertaining to the sterilization and cleanliness of the devices. Assess the impact of manufacturing related changes on the sterilization and cleanliness attributes of finished medical device products. Familiar with cGMP/cGDP, standard laboratory techniques (i.e. USP and ISO based testing methods) and safety procedures (i.e. OSHA). Knowledgeable in scientific concepts, measures, and terminology. Able to understand and apply specific laboratory protocols. Performs QA/QC duties as required. Responsibilities: -Author and execute protocols and final reports to assess impact of manufacturing related changes against cleanliness requirements for impacted medical devices. May provide analysis and evaluation of materials and products at all stages of development process. -Help manage the execution microbiological and chemistry testing both internally and externally. -Communicate and collaborate with project owners to obtain all necessary information for assessment. May entail communication with internal operations and/or external suppliers. -Conducts work in compliance with cGMP/cGDP, safety and regulatory requirements.
Skills
regulatory, regulatory submission, gmp, regulatory compliance, batching
Top Skills Details
regulatory,regulatory submission,gmp
Experience Level
Expert Level
Pay and Benefits
The pay range for this position is $65.00 - $80.00
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Mahwah,NJ.
Application Deadline
This position will be accepting applications until Jan 10, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
- Hiring diverse talent
- Maintaining an inclusive environment through persistent self-reflection
- Building a culture of care, engagement, and recognition with clear outcomes
- Ensuring growth opportunities for our people
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
Salary : $65 - $80
