Medical Writer

PSG Global Solutions; Chesterfield (MO); On-site; USD 70,000 - 90,000; Full time

Job summary

A leading global solutions provider in Missouri is seeking a talented technical writer to join their BRD organization within the Pharm Sci BTx team. The successful candidate will verify data in regulatory documents, assist with document tracking, and create drafts using existing templates. With a focus on detail-oriented work, this role requires at least 3-5 years of experience in technical writing and a scientific degree in fields such as Biology or Chemistry. Opportunities for training and career growth are provided.

Qualifications

• 3-5 years of experience in technical writing, preferably in regulatory documents.
• Experience in bioprocess or cell line development areas is desirable.

Responsibilities

• Assist with verification of data within regulatory documents or reports.
• Support bioprocess R&D teams in tracking document completion.
• Create drafts of new technical or regulatory documents.
• Assist authors in assembling, formatting, and proofreading content.

Skills

Excellent oral and written communications

Experience in technical writing of reports

Regulatory experience

Detail oriented

Education

BS or higher in Biology, Chemistry, Biochemistry, Molecular Biology, Engineering, or similar

Job description

At Real we're always looking for new and ambitious people to help deliver exceptional service levels, change the lives of the candidates we represent and partner with some of the world's best pharmaceutical, biotechnology and medical companies.

As specialists in recognising talent we pride ourselves on not just finding the best people for our client partners but on our ability to spot the best and brightest talent to work for us. We are also renowned for providing training and long-term career opportunities to help our employees be the best they can be, so they can continue to deliver the expertise Real has become famous for.

Relationships are at the heart of everything we do and ensure that our clients and candidates continue to work with us again and again. This ethos is also what shapes how we work as a business. We encourage and reward knowledge sharing and have various support networks and international forums to enable our employees to keep up-to-date with changes happening across their industries and share local insight to deliver true global perspectives.

Job Description

The BRD organization within the Pharm Sci BTx organization needs to hire a technical writer. This colleague will perform the following activities:

• Assist with verification of data within regulatory documents or reports.
• Support the bioprocess R&D (BRD) teams in tracking document completion, data verification strategies and completion of edits.
• Create drafts of new technical or regulatory documents using existing examples, templates or reports
• Assist Bioprocess team authors in assembling, formatting, and proofreading figures, tables and content.

Qualifications

SKILLS:

• Excellent oral and written communications with experience in technical writing of reports and/or regulatory documents
• Regulatory, GMP or Pharmaceutical experience, preferrably in bioprocess or cell line development areas is desirable
• Detail oriented

EXPERIENCE:

• 3-5 years

EDUCATION:

• Scientific Background; BS or higher Biology, Chemistry, Biochemistry, Molecular Biology, Engineering, or similar

Additional Information

All your information will be kept confidential according to EEO guidelines.

IF THIS IS THE JOB OPPORTUNITY FOR YOU GIVE ME A CALL AT 646-618-8925 ASAP!

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