Technical Writer

Integrated Resources Inc.; Andover (MA); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Prime de recommandation

Job summary

Une entreprise dynamique spécialisée en solutions de main-d'œuvre recherche un Technical Writer pour rejoindre son équipe. Le candidat retenu sera responsable de la rédaction, de la vérification de documents techniques et réglementaires, et de l'assistance aux équipes R&D. Une formation scientifique est nécessaire, ainsi qu'une expérience en rédaction technique dans le secteur biopharmaceutique.

Qualifications

• Expérience en rédaction technique de rapports et/ou documents réglementaires requise.
• Expérience pertinente de 3-5 ans exigée.
• Détail orienté, capable de travailler de manière indépendante et en équipe.

Responsibilities

• Assistance à la vérification des données dans des documents réglementaires.
• Soutenir les équipes R&D dans le suivi de l'achèvement des documents.
• Création de brouillons de nouveaux documents techniques ou réglementaires.

Skills

Communication écrite et orale

Rédaction technique

Précision

Compétence interpersonnelle

Compétence avancée en MS Office

Education

BS ou plus en Biologie, Chimie, Biochimie, Biologie Moléculaire, Ingénierie ou domaines connexes

Job description

Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.

Job Description

Position: Technical Writer

The BRD organization within the Pharm Sci BTx organization needs to hire a technical writer. Responsibilities include:

1. Assist with verification of data within regulatory documents or reports.
2. Support the bioprocess R&D (BRD) teams in tracking document completion, data verification strategies, and editing.
3. Create drafts of new technical or regulatory documents using existing examples, templates, or reports.
4. Assist Bioprocess team authors in assembling, formatting, and proofreading figures, tables, and content.
5. Prepare documents using Regulatory templates in Microsoft Word and Predict, and work within GDMS document management system.

Skills

• Excellent oral and written communication skills, with experience in technical writing of reports and/or regulatory documents.
• Regulatory, GMP, or Pharmaceutical experience, preferably in bioprocess or cell line development areas.
• Detail-oriented with strong interpersonal skills, ability to work independently, multi-task, and be a team player.
• Advanced proficiency in MS Office.

Background/Experience

• Scientific background; BS or higher in Biology, Chemistry, Biochemistry, Molecular Biology, Engineering, or related fields.
• 3–5 years of relevant experience.

Additional Information

Feel free to forward this email to colleagues who might be interested. We offer a referral bonus.

Thank you.

Kind Regards,

Clinical Recruiter

Integrated Resources, Inc.

Direct #: (650)-399-0891

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