https://JOBS.HKAA.COM/ en-us Position Summary

Key Responsibilities

• Engage in planning and coordination activities to facilitate repairs and maintenance in both plant and office facilities, as well as machines and equipment.
• Support routine, periodic, or special inspections to identify necessary repair and maintenance work, ensuring the prevention of breakdowns.
• Collaborate with teams to ensure the identification, acquisition, and kitting of parts, and the collection of tools, documentation, and procedures for work activities.
• Create detailed schedules for upcoming work associated with future shutdowns or maintenance, aligning them with the operations schedule to minimize equipment downtime.
• Work with requestors and peers to develop appropriate scopes for corrective maintenance job plans and efficient work execution.
• Consult with Subject Matter Experts (SMEs) and Maintenance Supervisors to assign specific durations to planned and forecasted preventive maintenance.
• Assist craftsman and support teams in determining if scope changes can be completed without disrupting the schedule.
• Lead work order schedule preparation for assigned area over shutdown, including progress meetings with Maintenance, Project Engineering, and Operations teams for monthly activities as well as yearly shutdown.
• Support assigned area through attendance at daily meetings and preparation of maintenance schedule.

Role Requirements/ Qualifications

• Applicant must have a bachelor's degree with 0+ years of experience; OR an associate's degree with 4 years of experience; OR a high school diploma (or equivalent) and 6 years of relevant experience
• Proficient computer skills in MS Project, CMMS, Excel, and other relevant software
• Strong written and verbal communication skills
• Ability to facilitate cross-functional meetings effectively
• Experience in planning and execution of maintenance tasks and activities

Nice-to-have/ Preferred

• Experience and understanding of industry equipment and technology principles, theories, and practices
• Knowledge and experience with continuous improvement change implementation
• Familiarity with planning and execution of maintenance tasks and activities
• Experience in data management and visualization
• Effective time management skills

]]> Tue, 13 Oct 2026 00:00:00 EDT 0 Key Responsibilities

• Lead or co-lead moderately complex projects, effectively managing time and resources.
• Apply skills and knowledge to contribute to departmental work and resolve moderately complex problems.
• Make decisions guided by policies in non-standard situations and operate independently in ambiguous scenarios.
• Work independently on assignments, seek guidance on complex issues, and review your own and others' work.
• Utilize judgment and experience to become a resource for others and mentor colleagues.
• Troubleshoot and resolve on-site issues, collaborating with site operations to ensure continuous audit readiness.
• Identify high-risk areas, implement improvements, and interface with engineering and technical operations to enhance processes.
• Manage changes in the area, guide operational teams, prepare resource forecasts, and identify improvement opportunities.
• Facilitate agreements between teams, lead clinical production efforts, and ensure timely, injury-free, and defect-free execution.
• Develop Operations Specialists' skills, review area Change Controls, strengthen compliance culture, and enforce safety regulations while sustaining lean management practices.

Role Requirements/ Qualifications

• BA/BS with at least 4 years of experience or MBA/MS with at least 2 years of experience or PhD/JD with any years of experience or associate's degree with at least 8 years of experience or high school diploma (or equivalent) with at least 10 years of relevant experience
• Demonstrated expertise in applying statistical methodologies to enhance manufacturing processes and quality control test methods
• experience in managing projects
• Proficiency in the MS Office Suite, including Word, Excel, PowerPoint, SharePoint, and Visio
• Exceptional verbal and written communication skills
• Strong presentation abilities

Nice-to-have/ Preferred

• Relevant pharmaceutical experience
• PMP certification will be a plus
• Experience in a GMP environment
• Previous management experience
• Strong problem-solving skills
• Ability to work collaboratively in a team environment

]]> Mon, 12 Oct 2026 00:00:00 EDT 0 Position Summary

Whether you are involved in the design and development of manufacturing processes for products or supporting maintenance and reliability, engineering is crucial to ensuring customers and patients receive the medicines they need, precisely when they need them. By collaborating with our forward-thinking engineering team, you'll play a key role in accelerating the delivery of medicines to the world. Your innovative ideas and proactive actions will help us imagine new possibilities and bring them to life, ensuring that vital medications reach those in need more swiftly and efficiently. Your contributions will be instrumental in enhancing manufacturing information systems, boosting success rates, and ensuring zero downtime. By integrating manufacturing processes, operational knowledge, equipment control, and data into cohesive systems, you will enforce seamless operations across various departments. Your dedication will be pivotal in meeting project objectives and goals, fostering a collaborative team environment, and driving your colleagues towards success.




Role Requirements/ Qualifications

• Bachelor's degree with any years of experience, Associate’s degree with 4 years of relevant experience, or a high school diploma (or equivalent) and 6 years of relevant experience
• Hands-on experience with engineering design and validation
• Must be familiar with DeltaV, BMS, and or Allen Bradley PLC
• Proficiency in structured query language
• Demonstrated organizational skills to meet project task deadlines effectively
• Excellent communication and interpersonal skills
• Experience with automated systems and equipment
• Knowledge of Good Manufacturing Practices

Nice-to-have/ Preferred

• Experience in pharmaceutical industry engineering
• Familiarity with Preventive Maintenance Procedures for process control systems
• Ability to monitor issues and develop preventative solutions
• Experience with manufacturing information systems
• Excellent judgment and decision-making skills

Key Responsibilities

• Deploy and test automated processes, systems, and equipment.
• Execute Good Manufacturing Practices and verification protocols.
• Monitor and identify issues to develop preventative solutions.
• Support the development of Preventive Maintenance Procedures for process control systems.
• Adhere to safe work practices consistently.
• Contribute to project milestones, organize work to meet deadlines, and communicate progress and issues to peers.
• Learn and apply basic team effectiveness skills within the immediate Work Team.
• Make decisions to resolve basic problems with limited options and decision-making authority, under supervisor's direction.
• Work in a structured environment using established procedures, seeking guidance from colleagues, with regular reviews for technical judgment, completeness, and accuracy, relying on the supervisor's judgment.

Non-Standard work schedule, travel or environment requirements

• Position requirements are typical for a manufacturing plant-based work environment with shop floor exposure in manufacturing and utilities.
• There are no unusual physical or mental requirements for this position.

]]> Fri, 09 Oct 2026 00:00:00 EDT 0 Position Summary:

Everything we do every day is driven by an unwavering commitment to delivering safe and effective products to patients. Our quality culture, rooted in science and risk-based compliance, is both flexible and innovative, always putting the customer first. Whether your role involves development, maintenance, compliance, or analysis through research programs, your contributions will be instrumental in ensuring that our products meet the highest standards of quality and safety.




Role Requirements/ Qualifications

• Applicant must have a bachelor's degree with at least 4 years of
   experience; OR a master's degree with at least 2 years of experience; OR a PhD with 0+ years of experience; OR as associate's degree with 8 years of experience; OR a high school diploma (or equivalent) and 10 years of relevant experience.
• Strong understanding of validation principles and practices
• Experience with FDA and EU regulatory requirements and guidelines for validation
• Experience with technical transfers
• Proficiency in project management and resource planning
• Ability to work independently and make decisions in ambiguous situations
• Excellent communication and interpersonal skills
• Proficiency in computerized systems and software applications

Nice-to-have/ Preferred

• Demonstrated process and/or cleaning validation experience in a biopharmaceutical/pharmaceutical GMP environment
• Additional experience in other areas of validation

Key Responsibilities

• Provide process validation troubleshooting support for all equipment/unit operations and processes on site related to Sanford's Vaccine or other products.
• Lead and/or participates in the planning, preparation and execution of process validations, including continued process verification, as well as supporting tech transfer activities and related projects. This includes generation of protocols and cleaning assessments, direct sampling of equipment, working with manufacturing to align sample schedules, understanding Delta V controls, and pulling data from LIMs.
• Lead or co-lead moderately complex projects, managing time and resources effectively while providing guidance
• Apply skills and discipline knowledge to contribute to departmental work and make decisions to resolve moderately complex problems
• Operate independently in ambiguous situations, determining objectives of assignments and seeking directional review when necessary
• Review your own work and potentially mentor others, exercising judgment and becoming a resource for colleagues
• Guide operational teams in project management, resource forecasting, and identifying areas for improvement in products, processes, or services
• Facilitate agreements between teams to achieve project goals and coordinate validation/qualification work, including plans, strategies, and risk assessments
• Review and approve change controls, ensuring validation impact assessments and appropriate testing to maintain validated states
• Collaborate with Operations, Quality, Technical groups, and other site/network groups to meet business and compliance requirements
• Think through issues and troubleshoot problems related to cleaning and processing, work with the investigations group to provide technical justifications, understanding changes to cleaning and process systems, and interact with regulatory authorities during audits.
• Provide technical support, participate in change control implementations, deliver validation training, and ensure compliance with company policies and government regulations

Non-Standard Work Schedule, Travel or Environment Requirements

Schedule is primarily day shift but may require off-shift work on occasions. The position may require working on the floor in manufacturing at times which will require a heightened safety awareness and aseptic gowning will be required.
]]> Thu, 08 Oct 2026 00:00:00 EDT 0 Automation Manager – Manufacturing Technology

Leads the Focus Factory’s automation team, overseeing networked data collection, monitoring, automated equipment, controls, SCADA, and computerized GMP systems. Responsible for the design, deployment, integration, qualification, maintenance, and compliance of automation systems while minimizing downtime. Manages projects, documentation, risk assessments, change controls, troubleshooting, hypercare, and ongoing system support. Leads resources, manages contractors, promotes innovation and continuous improvement, collaborates with the site Center of Excellence, and develops talent and a diverse automation workforce.

Role Requirements:

Applicant must have a bachelor's degree with at least 4 years of experience; OR a master's degree with at least 2 years of experience; OR a PhD with 0+ years of experience; OR as associate's degree with 8 years of experience; OR a high school diploma (or equivalent) and 10 years of relevant experience.

Knowledge of working with computers and associated applications such as MS Word, Excel, PowerPoint.

Broad experience in a pharmaceutical environment with a hands-on understanding of control and data acquisition systems, IT infrastructures, automated calibration and maintenance management systems

Experience in designing and implementing PLC, SCADA, OPC, Data Management or networked automated systems and electronic batch records.

Preferred:

Prior experience in a high regulated pharmaceutical or biotech manufacturing environment.

Demonstrated experience in project management to timelines and budgets.

Experience in troubleshooting issues to root cause and recommending and implementing effective corrective actions.

Ensure that proven practices are defined and understood by team members who have the responsibility to implement automation systems

Display excellent interpersonal effectiveness and communication skills (written and oral).

Manage capital projects from conceptual phases through equipment installations, cGMP compliance, commissioning, validation and continuous improvement.
]]> Tue, 06 Oct 2026 00:00:00 EDT 0 Position Summary

This position will support the Quality Assurance department by performing Quality Assurance activities related to supplier quality management associated with clinical and commercial product. Conducts programs designed to improve supplier performance, prepares/maintains quality assurance procedures to assure compliance with customer and/or government requirements. In addition, provides support for regulatory agency inspections, displays extensive knowledge of cGXP, functions as subject matter expert (SME) in supplier management, and provides leadership to other team members.
 Note: This role is an individual contributor and will have no direct reports.




2. Role Requirements/ Qualifications

• Applicant must have Bachelor's degree in Science/related field with at least 4 years of experience OR, Master's degree in Science/related field with more than 2 years of experience, OR a PhD in Science/related field with 0 years of experience, OR an Associate's degree with 8 years of experience, OR a High School Diploma (or Equivalent) and 10 years of relevant experience.
• Experience in manufacturing, quality or engineering in the biotech or pharmaceutical industry.
• Strong communication and organization skills required.

3. Nice-to-have/ Preferred

• Prior experience working with Quality Assurance, supplier management, and/or Supply Chain preferred. Knowledge in cGXP, materials, components, and supplier management.

4. Key Responsibilities

• Perform QA assessments and approvals for supplier management.
• Interpretation of cGXPs for the commercial and clinical environment.
• Able to resolve complex issues with minimal assistance from management.
• QA supplier management activities (supplier reassessments, quality agreements, audit reviews, risk assessments)
• QA support and approval for qualification of new suppliers and materials
• QA disposition of incoming materials, as applicable
• Organize and provide written and/or oral presentations of work with minimal input. Communicate status and provide performance metrics to the team and site management.
• Ability to identify issues, present complex problems with possible solutions, and actively take leadership or independent role to resolve complex issues
• Provide guidance/coaching to less experienced colleagues.
• Proactively promotes teamwork and motivates others to achieve team objectives.
• Participate in external agency audits
• Trains other team members on tasks
• Identify and implement improvements to the supplier management process and other Quality Systems
• Interfaces with other parts of the organization such as research and development groups. Able to work outside immediate subject area, supporting a wider range of customers of differing subject areas and locations.
• Represents Quality Assurance in cross-departmental/cross-site/cross-network meetings/summits.

]]> Tue, 06 Oct 2026 00:00:00 EDT 0 Job Description:




The Designer III (DT III) position is the third level in the Designer career track. This role provides designs for utility systems, including overhead and underground circuits for joint use, lighting, and commercial, industrial, and residential development. This track also supports field data collection and storm restoration efforts. You'll handle moderately complex design projects and provide support on more complex projects, with more independence than the DT II, while interacting with clients/customers and construction crews. Primarily office-based with significant field work required, including exposure to inclement weather.




Pay: $27.00–$30.00 per hour DOE




Responsibilities:




Independently perform field data collection and project-specific inspections for moderately complex projects

Produce high-quality CAD drawings and material lists for simple projects; provide support required by supervision for more complex tasks

Ensure all necessary project communications are documented as required by training

Provide guidance and training to peers and newer designers on simple projects

Independently produce permitting documentation as needed

Communicate with clients and participate in site meetings with oversight

Work independently, under supervision for mentorship, guidance, and training




Required:




High school diploma or equivalent + 4 years of relevant work experience, OR Associate's degree + 3 years of relevant work experience

Valid driver's license

Must pass pre-employment drug screening and background check; motor vehicle checks may be required based on position

#PowerDistribution #UtilityDesign #EngineeringJobs #CADDesign #ElectricalDistribution #UtilityJobs #FieldEngineering #StormRestoration #HiringNow #NowHiring #RaleighNCJobs #DesignEngineer

#LI-RS1
]]> Tue, 08 Sep 2026 00:00:00 EDT 0 This position will involve meeting with the public to discuss lighting demands based on company standards and requirements. Site visits to determine customer lighting demands for residential, business and subdivisions. Ability to identify and verify the utility infrastructure.

Duties will include formulating and designing an outdoor lighting plan to best meet the customers’ needs that is within the guidelines of the standards. Communication skills will be crucial for discussions with clients, customers, crews, and other agencies. There will be intermittent days of fielding and days in the office designing. Ability to maintain a balance between schedules is imperative. Considerable walking, as well as carrying equipment, staking poles and flagging routes onsite is required, Strong skills acknowledging and managing customer complaints and the ability to find resolutions is essential.

High school or equivalent (Required)

Associates or Bachelors in Engineering (Preferred)

Experience:

Electrical systems: 1 year (Preferred)
MicroStation: 1 year (Preferred)

Skills: (needed, but not required)
Excel
Word
MicroStation (highly recommended)
DocuSign

Job Knowledge:
Basic Knowledge of Electric Fundamentals

#DAK

Job Type: Full-time

Benefits:

• 401(k)
• Dental insurance
• Employee assistance program
• Flexible spending account
• Health insurance
• Health savings account
• Life insurance
• Paid time off
• Vision insurance

Education:

• High school or equivalent (Required)

Experience:

• Poleforeman: 1 year (Required)
• Power Distribution: 1 year (Required)
• BOUD: 1 year (Required)

]]> Thu, 05 Mar 2026 00:00:00 EST 0