Technical Services Associate (B.S. in Science/Engineering Degree required)

Technical Services Associate (Entry-Level) – Pharmaceutical Manufacturing

This role is ideal for recent graduates or early-career professionals in scientific or engineering disciplines who are interested in building a career in pharmaceutical Technical Services, Manufacturing Support, or Quality Systems.

About KVK Tech

KVK Tech is a U.S.-based generic and specialty pharmaceutical manufacturer committed to developing and producing high-quality, FDA-approved medicines that improve patients’ lives through accessibility and trust. Headquartered in Newtown, Pennsylvania, KVK Tech maintains all operations within the United States, ensuring quality and consistency through strict adherence to cGMP standards and regulatory compliance. Our commitment to excellence is reflected in our precision, reliability, and shared mission to provide safe, affordable, and life-improving pharmaceutical products.

What You’ll Do

The Technical Services Associate supports oral solid dosage (OSD) pharmaceutical manufacturing through technical documentation, batch record development, and quality system support activities. In this position, you will work closely with Manufacturing, Quality Assurance, Validation, Engineering, and Regulatory teams to ensure controlled documentation is accurate, compliant, and aligned with current manufacturing practices. You will gain hands-on exposure to batch record development, change control, investigations, and technical documentation within a cGMP-regulated environment.

Key Responsibilities:

• Author, revise, and maintain controlled documents including SOPs, work instructions, manufacturing and packaging batch records (MPRs/MPKs), and technical reports.
• Support the development and lifecycle management of manufacturing and packaging batch records to ensure clarity, usability, and compliance with cGMP and GDP standards.
• Draft and update documentation related to deviations, CAPAs, and change controls in collaboration with cross-functional subject matter experts.
• Assist with technical transfer and validation documentation under supervision of Technical Services leadership.
• Collaborate with Manufacturing and Engineering teams to ensure documentation accurately reflects approved processes, equipment, materials, and controls.
• Maintain document control standards including version control, formatting, periodic review support, and controlled distribution.
• Support inspection readiness by ensuring documentation is organized, current, and readily retrievable.

What We’re Looking For

Experience:

• 0–4 years of experience in pharmaceutical manufacturing, quality systems, validation, laboratory operations, or other regulated environments preferred.
• Internship, co-op, or academic project experience in a GMP or regulated environment strongly encouraged.
• Demonstrated ability to write clearly, organize technical information, and work with strong attention to detail.

Education:

• Bachelor’s degree in Pharmaceutical Sciences, Chemistry, Biology, Biochemistry, Chemical Engineering, Industrial Engineering, or related scientific/technical discipline required.
• Recent graduates are encouraged to apply.

Skills & Knowledge:

• Foundational understanding of cGMP and Good Documentation Practices (GDP) preferred.
• Strong technical writing and organizational skills.
• Ability to interpret technical information and collaborate effectively with cross-functional teams.
• Proficiency in Microsoft Office (Word, Excel, PowerPoint).
• Strong attention to detail and ability to manage multiple priorities in a structured environment.

What We Offer

• Competitive compensation
• Annual performance bonus eligibility
• Annual merit-based pay increases
• Automatic enrollment in a 401(k) at 3% pre-tax with 50% company match on the first 6% contributed
• Paid Time Off
• 10 paid company holidays
• Comprehensive medical, dental, vision, and life insurance coverage
• Professional development reimbursement
• Career growth opportunities within Technical Services, Validation, Quality, and Manufacturing
• Tuition reimbursement for children and childcare expense reimbursement

Schedule

• Full-time, on-site position (Monday–Friday, 8:00 AM – 5:00 PM)