Documentation & Validation Specialist, Site Associate

Documentation & Validation Specialist, Site Associate BWT Pharma & Biotech Inc. Marlborough, MA Job Details Full-time $58,000 - $65,000 a year 1 day ago Benefits Health insurance Dental insurance 401(k) Flexible spending account Tuition reimbursement Paid time off Parental leave Employee assistance program Vision insurance 401(k) matching Professional development assistance Life insurance Qualifications Microsoft Excel Microsoft Outlook Interpersonal skills Word embeddings Bachelor's degree Data entry Organizational skills Document viewing software Time management Full Job Description BWT Pharma & Biotech, a leading supplier of high purity water systems for leading pharmaceutical companies worldwide, seeks to employ an experienced Documentation & Validation Specialist. The role requires a candidate with strong organization and communication skills. The primary focus of this role is to work closely with Project Managers and Engineers to support project execution. This is a great opportunity for an experienced Documentation & Validation Specialist looking to expand their knowledge and understanding of complete project execution from design phase to final handover phase with customers. This will include first-hand experience with Factory Acceptance Tests and Site Acceptance Tests. This is a unique opportunity for candidates looking to progress their career that have a passion for being part of a dynamic team.

Job Responsibilities:

Prepare and maintain engineering documentation packages Maintain drawing and documentation control Component (equipment, instruments and valve) and material verification Management and verification of engineering BOMs from ERP system Enters and revises data in ERP system Co-ordinate project documentation flow from design stages to procurement to production Participation in FAT (Factory Acceptance Test) and SAT (Site Acceptance Test) Resolve issues through development of systems and procedures

Required Skills & Experience:

Minimum 2-3 years' experience within technical industry in similar role Ability to work carefully, methodically and consistently Strong verbal and written communication skills Familiarity with non-conformance logs and/or deviation reports preferred Proficient in Adobe Must be able to multi-task supporting various groups Proficient in Microsoft Word, Excel and Outlook Knowledge of pharmaceutical validation/documentation would be a key advantage. Planning and time management skills Familiarity with GDP (Good Documentation Practices) Willingness to travel at times for SAT client visits Personal Attributes Excellent interpersonal communication Professionalism in both in-office and client interactions Customer-service driven with attentive foresight Enthusiastic, self-motivated, ambitious and determined to succeed •Applicants must have unrestricted work authorization; sponsorship or visa transfers will not be provided.

Pay:

$58,000.00 - $65,000.00 per year

Benefits:

401(k) 401(k) matching Dental insurance Employee assistance program Flexible spending account Health insurance Life insurance Paid time off Parental leave Professional development assistance Tuition reimbursement Vision insurance

Education:

Bachelor's (Preferred)

Experience:

Documentation & Validation :

2 years (Required)

Location:

Marlborough, MA 01752 (Preferred) Ability to

Commute:

Marlborough, MA 01752 (Required) Willingness to travel: 25% (Required)

Work Location:

In person