Pharmatechniker mit Bachelor oder Master - Job Opportunity at By Your Site Personal GmbH & Co. KG

Vechta, Germany
Full-time
Mid-level
Posted: April 2, 2025
On-site
EUR 45,000 - 65,000 annually based on qualification level and experience

Benefits

Comprehensive Onboarding Program with Dedicated Support
Performance-Based Annual Christmas Bonus
Vermögenswirksame Leistungen (Employee Savings Benefit)
Company Pension Plan with Employer Contributions
Tax-Free Monthly Benefits Package
Up to 30 Days Annual Leave
Professional Development Programs
Work Anniversary Recognition Program
Personal Milestone Celebrations

Key Responsibilities

Lead and Execute Qualification/Validation Programs for Sterile and Solid Pharmaceutical Production
Strategic Cross-functional Team Coordination across Technical, Production, and Quality Departments
Development and Management of Critical Quality Documentation Systems

Requirements

Education

Bachelor's or Master's degree in Pharmaceutical Technology or related technical field

Required Skills

Proficiency in Microsoft Office Suite (Excel, Word, Outlook, PowerPoint) Fluent German and English communication skills Structured and independent work methodology Team collaboration and effective communication abilities
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Sauge AI Market Intelligence

Industry Trends

The pharmaceutical manufacturing sector is experiencing increased demand for validation specialists due to growing regulatory requirements and the expansion of sterile manufacturing facilities. Digital transformation in pharma manufacturing is driving need for technical expertise combined with GMP understanding. Rising focus on sterile manufacturing capabilities in Europe is creating competitive demand for qualified personnel.

Role Significance

Typically operates within a validation team of 5-8 specialists, coordinating with broader technical and quality teams of 20-30 people
Mid-level position with significant technical responsibility and cross-functional leadership requirements

Key Projects

Implementation of new production line validation protocols Quality system enhancement initiatives Cross-functional compliance projects Technical documentation system improvements

Success Factors

Strong understanding of GMP requirements and pharmaceutical manufacturing processes Excellent project management capabilities Ability to navigate complex regulatory requirements while maintaining operational efficiency Strong technical writing skills for documentation requirements

Market Demand

High demand with strong growth trajectory due to expanding pharmaceutical manufacturing sector in Germany and increasing regulatory requirements

Important Skills

Critical Skills

GMP knowledge and application in pharmaceutical manufacturing Technical documentation expertise Cross-functional team leadership Validation protocol development and execution

Beneficial Skills

Project management methodologies Risk assessment capabilities Quality management systems expertise Digital transformation knowledge

Unique Aspects

Combination of technical expertise with validation specialization
Strong focus on cross-functional team leadership
Emphasis on both sterile and solid form manufacturing expertise

Career Growth

2-4 years in role before advancement opportunity, depending on project success and organizational growth

Potential Next Roles

Senior Validation Specialist Validation Manager Quality Assurance Manager Technical Operations Lead

Company Overview

By Your Site Personal GmbH & Co. KG

By Your Site Personal GmbH & Co. KG operates as a specialized technical recruitment firm focusing on pharmaceutical and life sciences sectors

Regional leader in pharmaceutical industry staffing with strong connections to major manufacturers
Strong presence in Northern Germany with established relationships with key pharmaceutical manufacturers
Professional environment with emphasis on technical excellence and regulatory compliance
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Data Sources & Analysis Information

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  • Salary estimates and market demand analysis
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  • Critical success factors and key skills
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