Manufacturing Technician Job in GSK
Posted Date: Dec 20 2021
As a Manufacturing Associate you will perform duties as assigned with respect to quality, timeliness, quantity and cost. You will also work individually and as a team to deliver cGMP compliant product and adhere to GSK policies, procedures and support site goals.
Your responsibilities include some of the following:
Responsible for application of GSK safety and environmental guidelines and act as a role model within the department
Ensure all job responsibilities are in compliance with applicable regulations, current operating procedures and industry practice
Identify and help mitigate EHS and safety risks. Hazardous waste training depending on specific requirements of VS department
Complete documentation in line with regulatory, GSK, and departmental requirements
Work and communicate closely with other departments both inside and outside of the Value Stream
Ensure all activities are executed following quality and regulatory standards.
Supports cross-functional communication and the GSK quality mindset by proactively identifying and reporting compliance issues to area supervisor or QA. Work with supervisor and QA to mitigate identified issues
Participate in and support continuous improvement, and LEAN initiatives. Recognize technical issues and relay to supervisor
Represent GSK with the highest level of integrity and professionalism. Ability to maintain confidentiality of sensitive information. Adhere to GSK policies and procedures and support management decisions and goals in a professional manner. Show awareness of changing schedules, request and priorities put forth by management
The following GSK values and expectations are key behavioral characteristics for this role: Patient Focus, Transparency, Respect, and Integrity, Courage, Accountability, Development, and Teamwork
We are looking for professionals with these required skills to achieve our goals:
High School Diploma or equivalent
2+ yrs experience cGMP/Healthcare/Lab-related experience
Bachelors degree in related field
1+ yrs experience cGMP/Healthcare/Lab-related experience
If you have the following characteristics, it would be a plus:
Good verbal and written communication skills. Ability to communicate effectively and project a professional image when giving/taking information in person, in writing, or over the phone
Understanding of Microsoft Office (MS Word, MS Excel, MS Outlook)
Understanding of weights and volume measures
Ability to take initiative and prioritize tasks; good time management, problem prevention, and problem-solving skills
Perform manufacturing/cleaning/sampling/processing steps in coordination with other manufacturing/QA/QC personnel
Handling of hazardous waste from production activities to satellite storage areas. Annual training on area-specific hazardous waste handling as required. This training satisfies annual RCRA training requirement for large quantity generators and is part of the site’s RCRA compliance program
Maintain and review training forms and files
Participate in RCA for EHS incident and deviations
Participate in presenting and maintaining site in a state of inspection readiness
Responsible for participation in CAPA tasks both safety and quality related
Perform duties as per written procedures and maintain strict adherence to those procedures
Ask for assistance and does not perform duties without appropriate training
Attend all mandatory training and take a positive approach to compliance
Work both independently and in a team environment
Adapt to changing schedules, priorities, and requests from supervisor
Escalate issues and concerns (safety, quality, production) to supervisor
Our values and expectations are at the heart of everything we do and form an important part of our culture.
These include Patient focus, Transparency, Respect, Integrity along with Courage, Accountability, Development, and Teamwork. As GSK focuses on our values and expectations and a culture of innovation, performance, and trust, the successful candidate will demonstrate the following capabilities:
- Operating at pace and agile decision-making – using evidence and applying judgement to balance pace, rigor and risk.
- Committed to delivering high quality results, overcoming challenges, focusing on what matters, execution.
- Continuously looking for opportunities to learn, build skills and share learning.
- Sustaining energy and well-being
- Building strong relationships and collaboration, honest and open conversations.
- Budgeting and cost-consciousness
- This is a job description to aide in the job posting, but does not include all job evaluation details.
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Last Date For Apply: 23/Mar/2022 00:00:00 Job Type : Full Time, Employment Type : Apply Here