Job Type

Contractor

Posted

15 days ago

Location

Thousand Oaks, CA

Description

Our client, a world-leading Pharmaceutical Company in Thousand Oaks, CA is currently looking for a Regulatory Affairs Associate I / Pharma Industry to join their expanding team.

Position Details:
  • Job Title: Regulatory Affairs Associate I / Pharma Industry
  • Duration: 12 months contract, extendable up to 36 months
  • Location: Thousand Oaks, CA

Note:
  • The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
  • You may participate in the company group medical insurance plan

Job Description:
  • Candidate will be remote then required to be on site once it re opens
  • Must have Pharma Biotech experience
  • Please submit candidates at market rate for review. Please be mindful of SR role and this should not exceed based off experience

Responsibilities:
  • The Associate Regulatory Affairs (CMC) role is an entry level regulatory position that provides varying levels of product support to the regulatory Chemistry, Manufacturing and Controls (CMC) department, across regions and phases of development.
  • Support may include organizing, managing and executing on regulatory CMC projects in support of regulatory submissions.
  • Tasks may include formatting of documents per style guide, searching for and organizing data from regulatory repository systems, drafting meeting agendas and minutes, managing document reviews, and other tasks as requested.
  • What we are looking for:
  • Desire to learn Regulatory Affairs CMC and global submission strategy;
  • Strong organizational skills with attention to detail;
  • Proficient time management skills and ability prioritize workload;
  • Ability to work both independently and as a member of a team;
  • Proficient skills in Microsoft Office suite, especially Word, Excel, PowerPoint and Project;
  • Qualified to work in the U.S. without employer sponsorship;
  • Commitment of a 40-hour work week in Thousand Oaks, California

Requirement:
  • Bachelor's or Master's degree with 1 to 2 years of either Regulatory, Compliance, Quality, Biopharmaceutical, Pharmaceutical or related scientific experience OR
  • Associate degree and 6 years of either Regulatory, Compliance, Quality, Biopharmaceutical, Pharmaceutical or related scientific experience OR
  • High school diploma / GED and 8 years of either Regulatory, Compliance, Quality, Biopharmaceutical, Pharmaceutical, and/or related scientific experience
  • Degree in life sciences, biochemistry, or chemistry
  • Experience in biopharmaceutical or pharmaceutical industry
  • Familiarity with eCTD structure
  • Motivated with initiative to learn quickly
  • Experience in CMC, including preparation of submissions to Agencies
  • Proficient skills in Microsoft Office suite, especially Word, Excel, PowerPoint and Project

Top 3 Must Have Skill Sets:
  • Must have pharma/biotech experience, must have experience in some part of the drug manufacturing process (Manufacturing, QC/QA, analytical experience, etc.)
  • Can-do Attitude – Ideal candidate does not easily give up. The candidate will be provided direction and support but will need to be methodical and analytical when completing tasks while exhibiting a positive attitude (Client is a very large organization and there will be many parties the candidate will need to engage with for project success).
  • Being Comfortable With Being Uncomfortable – Ideal candidate will not only be able to identify problems but also identifies possible solutions. Project end goals will be known but all the in-between steps may not be known from the start so the candidate will need to navigate and structure the steps without being easily flustered.
  • Attention to Detail – Ideal candidate will be thorough and deliver polished work product.

Day to Day Responsibilities:
  • This is a very task oriented role-Daily responsibilities will be focused on providing submission execution support to products across modalities, regions and phases of development

Employee Value Proposition:
  • You will work directly with project teams in support of submission execution.
  • The projects you will be involved with will have a positive impact on key Client processes that support the making of human therapeutics and the patients that use them.

Red Flags:
  • Over qualified candidate-this is an entry level regulatory position
  • Unexplainable time gaps in resumes

About the Company

Company Logo Pioneer Data Systems
Company Logo Pioneer Data Systems
Company Logo Pioneer Data Systems
Company Logo Pioneer Data Systems

Pioneer Data Systems

Delivering professional consulting services since 1995. Our original area of focus was providing professional services for Oracle databases. As a market leader, we were recognized as a "New Jersey Technology Fast 50" company by Deloitte & Touche. Pioneer is a certified Minority Business Enterprise (MBE) and a recipient of Inc500 award for America's fastest growing private businesses. Over the years we have leveraged our expertise in the IT space and have diversified across market sectors, now catering to a wide range of practice areas, including Pharmaceutical / Clinical Research, Scientific, Engineering, Accounting and Finance. Many of our clients include Fortune 500 companies that have been trusting us to deliver the highest quality talent for well over a decade. Our strategic offshore location in Pune, India, allows us to take advantage of world time-tables, to offer the highest quality services around the clock. For further information on how our innovative delivery model can enhance your bottom-line, check out section Reduced Cost Per Hire. Our clients can rest assured our dedicated recruiting teams around the globe are committed 24 hours a day to driving forward our mission of acquiring the very best available talent for their staffing needs.

Company Size

50 to 99 employees

Industry

Biotechnology/Pharmaceuticals

Founded

1995

Website

http://www.pioneerdata.com/