Scientist II

Description:

INTAKE NOTES:



Pay Rate: $55-$57

- On-Site is strongly preferred. Flexibility can be discussed based on qualifications but the candidate should be located with 50miles of Hologic SD

-Skill sets that are a "must have" and/or information about the position that the suppliers should be aware of to recruit for this role: Strong communication skills, this person will be expected to reach out both within our department and cross functionally to ensure timely input to regulatory responses

-Extension possible; not guaranteed



Skillset Matrix Manager Notes:

Technology Requirements (I.E Programs, systems, etc): Microsoft (Outlook, Teams, Sharepoint, Planner)

Agile

Oracle

JMP



What does a typical day look like? (daily tasks) Tracking of activities and deliverables

Documentation search and review

Regulatory Response preparation and review

Knowledge gathering and organization



Preferred background/prior work experience? IVD molecular diagnostic Assay Product Development



Priority soft skills Organized, communication







Specific Duties

Job Title: Temporary Scientist II R&D Assay Development, On-Market Support (Global Regulatory Submissions)

Location: [Insert Location]

Duration: 1 Year, Full-Time (40 hours/week)

Reports to: R&D Assay Development On-Market Support Team Lead

Position Summary:

We are seeking a motivated and detail-oriented Scientist II (Senior Scientist equivalent) for a one-year temporary assignment within our R&D Assay Development On-Market Support team. This role is dedicated to supporting global regulatory submissions for our on-market products. The successful candidate will be responsible for project management, regulatory response coordination, and documentation strategy, contributing directly to the continued success of our product portfolio.

Key Responsibilities:

Regulatory Submission Support:

Coordinate and deliver timely, informed responses to global regulatory authorities questions related to assay development and product performance.

Collaborate cross-functionally with Regulatory Affairs, Quality, and R&D teams to gather and synthesize necessary information for submissions.

Project Management:

Track and manage activities and deadlines related to regulatory submissions and post-market support projects.

Maintain project timelines and communicate status updates to stakeholders.

Product Knowledge Repository:

Establish and maintain a comprehensive repository of product knowledge, including technical documentation, study data, protocols, and regulatory correspondence.

Ensure the repository is organized, accessible, and up-to-date for internal use.

Documentation Strategy:

Assess current documentation and design history files for completeness and regulatory readiness.

Make recommendations and develop strategic plans to address gaps, including proposing new study plans, protocols, and documentation updates.

Partner with subject matter experts to drive documentation improvements and ensure compliance with global regulatory requirements.

Qualifications:

PhD or MS in life sciences, chemistry, biochemistry, or related field (or equivalent experience).

3+ years of experience in assay development, R&D, or related scientific role; experience in regulated environments preferred.

Demonstrated experience supporting global regulatory submissions or working with regulatory authorities.

Strong organizational and project management skills, with the ability to manage multiple deadlines and priorities.

Excellent written and verbal communication skills.

Ability to synthesize complex scientific information for a variety of audiences.

Experience with documentation systems, design history files, and regulatory documentation standards.

Proficiency in Microsoft Office and project management tools.

Preferred Qualifications:

Previous experience in on-market support for medical devices, diagnostics, or related regulated products.

Familiarity with global regulatory requirements (e.g., FDA, CE, PMDA).

Experience in establishing knowledge repositories or databases.

Employment Type:

Temporary, Full-Time (40 hours/week), 1 Year







General Summary of Duties and Responsibilities:

Candidates should have experience working in a GMP environment.



- Plans and executes own experimental work

- Analyzes associated lines of investigation and devises and recommends methods to resolve problems

- Writes reports covering data and scientific explanation of results and conclusions

- Collaborates outside team on project related issues or studies



Qualifications To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the basic knowledge, skills, and or abilities required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

- Solid knowledge of molecular biology, chemistry, biochemistry or related disciplines

- Understanding of molecular diagnostic technology and nucleic acid amplification

- Understanding of scientific method experimental design and statistical analysis

- Ability to design both standard and factorial experiments process improvement

- Ability to analyze data and come to valid scientific conclusions,

- Ability to prepare and present studies to small groups of people

- Sound technical writing skills and ability to document technical work.

- Ability to communicate effectively with peers and management.

Experience working in a GMP environment