Beigene
From Beigene's careers page
Status: listed on the employer's own careers page when we last checked (daily). Confirm on their site before applying.
BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.
The Manufacturing Support Coordinator role is a non - exempt position responsible for supporting the following activities but not limited to:
Developing and maintaining the document management process for Drug Substance and Drug Product manufacturing teams.
Ensure compliance within the document management system, document issuance, reconciliation, retention when in use within department, and final storage.
The coordinator will ensure that the organizational documents are prepared, maintained, distributed, updated, and stored according to the organization’s document management standards.
Besides document management other responsibilities may include material management such coordinating of materials with supply chain, maintenance of training records for the teams, authoring of deviations and change controls. Other responsibilities may be added as needs of the department may expand.
Minimum of 4 years biopharmaceutical manufacturing experience.
Bachelor’s Degree: Science / Engineering or equivalent experience in biopharmaceutical industry.
Support Document Management Operations team
Oversee revision control
Scan and file documents
Supporting project tasks
Supporting the Material Specification project team
Processing controlled documentation within the customers system
Formatting to structure record and data entry work
Advising and responding to queries on document status by interfacing with operation management
Demonstrated ability to successfully gown into aseptic manufacturing areas
Excellent organization and time-management skills required
Must be able to manage heavy workload and aggressive timelines in a timely manner, prioritize and work under pressure
Strong work ethic, Positive Attitude, Time Management, Problem Solving, Team Player, Self Confidence & Ability to Accept & apply Lessons Learned as needed
Works with a sense of urgency, while engaging and listening to experts
Ability to work in a fast-paced environment while demonstrating excellent time management and organization skills
Strong organizational skills with the proven ability to prioritize
Must be dependable and punctual
Proficient in the use of standard Microsoft Office software products, including Excel, Outlook, Word
Must be flexible to work 1st or 2nd shift with holidays, weekends and overtime as per business needs
Customer/Client Focus
Issuance of batch related documentation and labels in support of GMP manufacturing.
Reconcile GMP documentation following document lifecycle requirements.
Creation and issuance of GMP logbooks/notebooks.
Responsible for storage and archival of GMP documents and batch related records.
Perform tasks in a manner consistent with the safety policies, quality systems and cGMP requirements.
Drive continuous improvement.
Support Document Management Operations team.
Oversee revision of Batch record, protocol and other control documents.
Scan and file documents.
Supporting project tasks.
Processing controlled documentation within applicable system.
Formatting to structure and formatting control record and data entry work.
Advising and responding to queries on document status by interfacing with operation management.
Responsible for the administration and management of Facilities Engineering records in an effective and efficient method within HPW facility.
Prepare and organize documentation procedures following.
Assist departments with equipment and system documentation. Coordinate system implementation and prepare documentation as necessary.
Identify specific process improvement as needed and provide recommendations concerning established workflows.
Work directly with Document Management, Drug Substance, Drug Product, Warehouse, and various Quality organizations.
Maintain open communication with management, co-workers, customers and counterpart staff in other sites.
Manage all Turn-Over-Packages (TOP) and Commissioning Packages from HPW site projects.
Maintain open communication with management, co-workers, customers, and counterpart stain in other sites as needed (GZ).
Maintain close collaboration with QA, QC, DP, DS and WH operations.
Material Staging and support with reservations within SAP system for Drug Substance and Drug Product
Managing workflows and metrics for manufacturing areas.
Must attend both the DS and DP, morning huddles.
Works in a collaborative team setting with quality counterparts that include Manufacturing Operations, Engineering and Validation, Quality Control, Quality Assurance Manufacturing, Supply Chain and Warehouse.
Manage all Turn-Over-Packages (TOP) and Commissioning Packages from HPW site projects.
Maintain open communication with management, co-workers, customers, and counterpart stain in other sites as needed (GZ).
Work with Supply Chain to coordinate the manufacturing schedule to support the batch records, labels and forms requirements prior to the start of production.
The position will be trained and may also support the following on the manufacturing floor areas as needed basis:
Master Batch Records, Logbooks, Forms, Labels etc are all stored in the designated are on the manufacturing floor at least 2 days prior to the production run. Material Staging and room readiness.
Master Batch Records, Logbooks, Forms, Labels etc. are all stored in the designated are on the manufacturing floor at least 2 days prior to the production run.
Weigh and dispense Documentation and SAP reservation, Materials readiness prior to campaign start.
Workflow and process alignment for all documentation issuance including labels, Master batch records, SOPs, Work instructions, Forms, etc.
Must be able to stand for long periods, up to 8 to 12 hours/day.
Must be able to reach above shoulder level, bend/stoop, push/pull, and handle/grip frequently.
Must be able to work scheduled 40 hours with the ability to work overtime as needed.
Must be comfortable in working in varying temperatures.
Frequent lifting, pushing, pulling, and carrying. Ability to lift to 40 lbs.
Regular reaching, bending, stooping, and twisting.
Repetitive motion and substantial movement of the wrists, hands, and/or fingers.
Environment requires dedicated gowns, depending on area.
Work with hazardous materials and chemicals.
Availability to work off shift hours and weekends on occasion.
Global Competencies
When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.
Fosters Teamwork
Provides and Solicits Honest and Actionable Feedback
Self-Awareness
Acts Inclusively
Demonstrates Initiative
Entrepreneurial Mindset
Continuous Learning
Embraces Change
Results-Oriented
Analytical Thinking/Data Analysis
Financial Excellence
Communicates with Clarity
Salary Range: $29.13 - $41.13 per hour BeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process. Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.
We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans’ Readjustment Assistance Act of 1974, Title I of the Americans with Disabilities Act of 1990, and any other applicable federal, state or local laws, applicants who require reasonable accommodation in the job application process may contact accommodationsus@beonemed.com.
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