Quality Assurance Inspector 3rd shift

We need to produce HTML fragment with sections only if real content. Use

for headings: About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. We must not repeat job title. No Job ID. Remove boilerplate. We need to parse the posting. Key info: - Work Schedule: Third Shift (Nights) (Shift: 3rd shift Sunday 11PM - Friday morning 7AM). Also later: "Work schedule, Monday through Friday, 8 hours per day." There's some conflict: earlier says third shift Sunday 11PM - Friday morning 7AM. Later says Monday through Friday 8 hours per day. We need to preserve all substantive info. So schedule info: Third Shift (Nights) Sunday 11PM - Friday morning 7AM; also Monday through Friday 8 hours per day; additional overtime and weekend may be required. - Environmental Conditions: many details: GMP safety standards, cleanroom restrictions, cold room/freezers -22°F/-6°C, loud noises, PPE required, no contact lens allowed; prescriptive glasses provided. Also later: "This job requires the incumbent to work in a refrigerated environment (2° C to 8° C) and freezer environment (-20° C) with provided protective wear." Also "The position is exposed to cold temperatures for more than one hour at a time. The position is exposed to -20F temperatures for at least 15 minutes at a time." - About the role: description: "As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer." - DESCRIPTION: "Join our team at Thermo Fisher Scientific as a Lead QC Technician, where you'll help make the world healthier, cleaner and safer. In this important role, you'll ensure quality standards are met through inspection of products in a cGMP environment. The Operations, Clinical Quality Assurance Inspector will support all Quality functions in relation to packaging activities of clinical product processed through primary and secondary packaging operations. Support of commercial packaging activities is also included. The role involves supporting management and the quality team and close interaction with relevant cross functional groups at the site. The role requires the ability to problem solve and effectively ensure the site follows established quality systems. Additionally, the role requires strong communication skills both verbally and written. Candidate should have experience with cGMP regulations." - REQUIREMENTS: list bullet points: Applies Good Manufacturing Practices (cGMP) in all areas of responsibility. Demonstrates and promotes the company vision. Performs approval of specifications and Incoming Inspections on material (i.e. drug, components) and distribution shipments. Performs material and process inspections and samplings. Review and approve Packaging Electronic Production Orders. Participates in continuous improvement initiatives and assists with root cause investigations for nonconforming issues. Author's, revises and follows all relevant SOP's/Work Instructions and accurately documents activities as needed. Resolve and assure that issues potentially affecting product quality/compliance are raised to the attention of the Team Leader and/or Management. Assures that issues are resolved in a timely manner and corrective actions are implemented accordingly. Performs all activities in a safe and efficient manner. Other duties may be assigned to meet business needs. - Keys to Success: Education Associates degree preferred. High School Diploma, or equivalent required. Experience At least 2 years of experience in Pharmaceutical, or related regulated industry. Knowledge, Skills, Abilities: A minimum of 1 year of experience in Pharmaceutical or in a related, regulated industry and a High School diploma. Familiar with Quality Systems (Change Control, Deviations, Complaint Management, Documentation Management, among others). This job requires the incumbent to work in a refrigerated environment (2° C to 8° C) and freezer environment (-20° C) with provided protective wear. Must be willing to work various shifts and overtime depending on business needs. Ability to work independently. Skills required; to read, understand, and follow the SOP's, Work Instructions and policies of a GMP environment. - Physical Requirements: Extensive standing and walking on packaging floor in order to monitor room activities. Work schedule, Monday through Friday, 8 hours per day. Additional overtime and weekend (Saturday or Sunday) work may be required. This position requires standing, bending and lifting. Exerting and lifting to 25lbs of materials occasionally, and 10lbs of materials regularly. The position is exposed to cold temperatures for more than one hour at a time. The position is exposed to -20F temperatures for at least 15 minutes at a time. The position will be exposed to atmospheric conditions could require special personal protection equipment. Position is responsible for inspection of pharmaceutical products, components, and labels. Incumbent must meet applicable visual acuity/color blindness standards to perform visual inspections in a cGMP environment. We need to decide sections: About the role (description), Responsibilities (maybe from DESCRIPTION?), Requirements (list), Qualifications (education/experience), Skills (knowledge, skills, abilities), Benefits (none given), Pay (none), Schedule (work schedule). We should only include sections with real content. We have About the role: we have two paragraphs: the generic mission statement and the DESCRIPTION. Could combine. Responsibilities: The REQUIREMENTS list seems like duties/responsibilities. Could treat as Responsibilities. Qualifications: Education and experience requirements. Skills: Knowledge, Skills, Abilities. Schedule: Work schedule details. Benefits: none. Pay: none. We must not create sections with placeholder like "not specified". So omit Benefits and Pay. We need to preserve all substantive info. Ensure we don't lose any details. Let's craft HTML:

About the role

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

Join our team at Thermo Fisher Scientific as a Lead QC Technician, where you'll help make the world healthier, cleaner and safer. In this important role, you'll ensure quality standards are met through inspection of products in a cGMP environment. The Operations, Clinical Quality Assurance Inspector will support all Quality functions in relation to packaging activities of clinical product processed through primary and secondary packaging operations. Support of commercial packaging activities is also included. The role involves supporting management and the quality team and close interaction with relevant cross functional groups at the site. The role requires the ability to problem solve and effectively ensure the site follows established quality systems. Additionally, the role requires strong communication skills both verbally and written. Candidate should have experience with cGMP regulations.

Responsibilities

• Applies Good Manufacturing Practices (cGMP) in all areas of responsibility.
• Demonstrates and promotes the company vision.
• Performs approval of specifications and Incoming Inspections on material (i.e. drug, components) and distribution shipments.
• Performs material and process inspections and samplings.
• Reviews and approves Packaging Electronic Production Orders.
• Participates in continuous improvement initiatives and assists with root cause investigations for nonconforming issues.
• Author's, revises and follows all relevant SOP's/Work Instructions and accurately documents activities as needed.
• Resolves and assures that issues potentially affecting product quality/compliance are raised to the attention of the Team Leader and/or Management.
• Assures that issues are resolved in a timely manner and corrective actions are implemented accordingly.
• Performs all activities in a safe and efficient manner.
• Other duties may be assigned to meet business needs.

Qualifications

• Education: Associates degree preferred; High School Diploma, or equivalent required.
• Experience: At least 2 years of experience in Pharmaceutical, or related regulated industry.

Skills

• Familiar with Quality Systems (Change Control, Deviations, Complaint Management, Documentation Management, among others).
• Able to work in a refrigerated environment (2° C to 8° C) and freezer environment (-20° C) with provided protective wear.
• Must be willing to work various shifts and overtime depending on business needs.
• Ability to work independently.
• Skills required to read, understand, and follow the SOP's, Work Instructions and policies of a GMP environment.

Schedule

• Work Schedule: Third Shift (Nights) – Sunday 11PM – Friday morning 7AM.
• Standard work schedule: Monday through Friday, 8 hours per day.
• Additional overtime and weekend (Saturday or Sunday) work may be required.

We also need to include Environmental Conditions? Not a heading but could be part of About the role or Responsibilities? The posting includes environmental conditions details. We must preserve all substantive info. Where to place? Could add a section "Working Conditions" but not in allowed headings list. The allowed headings are only those specified. We cannot create new headings beyond those. So we must fit environmental conditions into existing sections. Perhaps incorporate into Responsibilities or About the role? The instructions: Use

for section headings (e.g. About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule). It says e.g., implying those are examples but we should use those headings. It says "Use

for section headings (e.g. About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule)." Likely we should only use those headings. So we need to embed environmental conditions somewhere, maybe under Responsibilities as bullet points, or under Skills. Since environmental conditions are not exactly responsibilities but could be part of "Working Conditions". But we have no heading for that. We could add them under Responsibilities as bullet points like "Adheres to GMP safety standards, cleanroom restrictions, etc." That would preserve info. Let's extract environmental conditions bullet points: - Adherence to all Good Manufacturing Practices (GMP) Safety Standards. - Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed. - Cold Room/Freezers -22degreesF/-6degrees C. - Loud Noises (Equipment/Machinery). - Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.). - No contact lens allowed; prescriptive glasses will be provided. - Works in refrigerated environment (2° C to 8° C) and freezer environment (-20° C) with provided protective wear. - Position exposed to cold temperatures for more than one hour at a time. - Position exposed to -20F temperatures for at least 15 minutes at a time. - Position may be exposed to atmospheric conditions requiring special PPE. We can incorporate these as bullet points under Responsibilities or maybe under Skills. Since they are conditions, maybe better under Responsibilities as part of duties (ensuring compliance). Let's add them as bullet points under Responsibilities after the existing list. We must not duplicate lines; there were duplicate lines in the posting; we need to preserve but not duplicate. We